Related gene-specific medical variations for Gene (Select 649) - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3134496	NM_006129.5(BMP1):c.1578G>C (p.Trp526Cys)	BMP1, LOC113788269 (W526C)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 3134495	NM_006129.5(BMP1):c.1374C>A (p.Ser458Arg)	BMP1, LOC113788269 (S458R)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 3134494	NM_006129.5(BMP1):c.1373G>T (p.Ser458Ile)	BMP1, LOC113788269 (S458I)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 3134493	NM_006129.5(BMP1):c.1366C>T (p.Arg456Trp)	BMP1, LOC113788269 (R456W)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 3019989	NM_006129.5(BMP1):c.1728C>T (p.Pro576=)	BMP1, LOC113788269	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 3017270	NM_006129.5(BMP1):c.1407G>A (p.Glu469=)	BMP1, LOC113788269	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 3007988	NM_006129.5(BMP1):c.1444-20G>A	BMP1, LOC113788269	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 3006245	NM_006129.5(BMP1):c.1647C>T (p.Asp549=)	BMP1, LOC113788269	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 3005374	NM_006129.5(BMP1):c.36G>T (p.Gly12=)	BMP1, LOC129999976	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 3001289	NM_006129.5(BMP1):c.1683G>A (p.Gln561=)	BMP1, LOC113788269	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 3000243	NM_006129.5(BMP1):c.148+13del	BMP1, LOC129999976	Deletion (intron variant)	not provided	GBenign
Select item 3000233	NM_006129.5(BMP1):c.1314T>C (p.Asp438=)	BMP1, LOC113788269	Single nucleotide variant (non-coding transcript variant +1 more)	not provided	GLikely benign
Select item 2996603	NM_006129.5(BMP1):c.1698C>T (p.Thr566=)	BMP1, LOC113788269	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2995828	NM_006129.5(BMP1):c.1444-9G>A	BMP1, LOC113788269	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2994087	NM_006129.5(BMP1):c.148+14G>A	BMP1, LOC129999976	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2993867	NM_006129.5(BMP1):c.1722T>C (p.Cys574=)	BMP1, LOC113788269	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2993724	NM_006129.5(BMP1):c.60C>A (p.Gly20=)	BMP1, LOC129999976	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2993707	NM_006129.5(BMP1):c.1692C>T (p.Leu564=)	BMP1, LOC113788269	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2993204	NM_006129.5(BMP1):c.148+16C>T	BMP1, LOC129999976	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2991946	NM_006129.5(BMP1):c.1425C>T (p.Leu475=)	BMP1, LOC113788269	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2990468	NM_006129.5(BMP1):c.1440T>C (p.Phe480=)	LOC113788269, BMP1	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2988174	NM_006129.5(BMP1):c.1455C>T (p.His485=)	BMP1, LOC113788269	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2987540	NM_006129.5(BMP1):c.1A>G (p.Met1Val)	BMP1, LOC129999976 (M1V)	Single nucleotide variant (missense variant +2 more)	not provided	GPathogenic
Select item 2983113	NM_006129.5(BMP1):c.1749C>T (p.Asp583=)	BMP1, LOC113788269	Single nucleotide variant (non-coding transcript variant +1 more)	not provided	GLikely benign
Select item 2980672	NM_006129.5(BMP1):c.1444-10C>T	BMP1, LOC113788269	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2980307	NM_006129.5(BMP1):c.1444-18T>A	BMP1, LOC113788269	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2980022	NM_006129.5(BMP1):c.21G>C (p.Leu7=)	BMP1, LOC129999976	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2979172	NM_006129.5(BMP1):c.1765+9C>T	BMP1, LOC113788269	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2978261	NM_006129.5(BMP1):c.120C>T (p.Pro40=)	BMP1, LOC129999976	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2975228	NM_006129.5(BMP1):c.1765+11C>G	BMP1, LOC113788269	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2975068	NM_006129.5(BMP1):c.1356A>G (p.Pro452=)	BMP1, LOC113788269	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2971040	NM_006129.5(BMP1):c.148+21del	BMP1, LOC129999976	Deletion (intron variant)	not provided	GBenign
Select item 2967917	NM_006129.5(BMP1):c.1349A>G (p.Asn450Ser)	LOC113788269, BMP1 (N450S)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2966890	NM_006129.5(BMP1):c.1640-20C>A	BMP1, LOC113788269	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2965521	NM_006129.5(BMP1):c.148+13C>T	BMP1, LOC129999976	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2964962	NM_006129.5(BMP1):c.1765+14G>T	BMP1, LOC113788269	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2961466	NM_006129.5(BMP1):c.1470C>T (p.Tyr490=)	BMP1, LOC113788269	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2959171	NM_006129.5(BMP1):c.1298-8C>T	BMP1, LOC113788269	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2955623	NM_006129.5(BMP1):c.1443+15C>T	BMP1, LOC113788269	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2919543	NM_006129.5(BMP1):c.1488C>T (p.Arg496=)	BMP1, LOC113788269	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2909882	NM_006129.5(BMP1):c.1359C>T (p.Asp453=)	BMP1, LOC113788269	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2907636	NM_006129.5(BMP1):c.1509C>T (p.Ser503=)	BMP1, LOC113788269	Single nucleotide variant (synonymous variant +1 more)	not provided	GBenign
Select item 2898183	NM_006129.5(BMP1):c.1734C>T (p.Tyr578=)	BMP1, LOC113788269	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2892224	NM_006129.5(BMP1):c.61C>A (p.Arg21=)	BMP1, LOC129999976	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2889505	NM_006129.5(BMP1):c.36G>A (p.Gly12=)	BMP1, LOC129999976	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2888158	NM_006129.5(BMP1):c.1390C>A (p.Arg464=)	BMP1, LOC113788269	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2887168	NM_006129.5(BMP1):c.1668C>T (p.Arg556=)	BMP1, LOC113788269	Single nucleotide variant (synonymous variant +1 more)	not provided +1 more	GLikely benign
Select item 2878360	NM_006129.5(BMP1):c.1752G>A (p.Lys584=)	BMP1, LOC113788269	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2876805	NM_006129.5(BMP1):c.1298-20C>A	BMP1, LOC113788269	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2872753	NM_006129.5(BMP1):c.1551C>T (p.Asp517=)	BMP1, LOC113788269	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2871934	NM_006129.5(BMP1):c.1449G>A (p.Glu483=)	BMP1, LOC113788269	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2868098	NM_006129.5(BMP1):c.148+13dup	BMP1, LOC129999976	Duplication (intron variant)	not provided	GBenign
Select item 2864012	NM_006129.5(BMP1):c.1298-20C>G	BMP1, LOC113788269	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2862233	NM_006129.5(BMP1):c.1392G>C (p.Arg464=)	BMP1, LOC113788269	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2861653	NM_006129.5(BMP1):c.1704C>T (p.Gly568=)	BMP1, LOC113788269	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2860285	NM_006129.5(BMP1):c.30G>A (p.Leu10=)	BMP1, LOC129999976	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2860085	NM_006129.5(BMP1):c.1512C>T (p.Thr504=)	BMP1, LOC113788269	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2845651	NM_006129.5(BMP1):c.1539G>A (p.Glu513=)	BMP1, LOC113788269	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2829335	NM_006129.5(BMP1):c.1689C>T (p.Cys563=)	BMP1, LOC113788269	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2823842	NM_006129.5(BMP1):c.1743C>T (p.Ala581=)	BMP1, LOC113788269	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2822935	NM_006129.5(BMP1):c.48C>A (p.Leu16=)	BMP1, LOC129999976	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2816520	NM_006129.5(BMP1):c.1639+12G>C	BMP1, LOC113788269	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2814845	NM_006129.5(BMP1):c.1344G>C (p.Ser448=)	BMP1, LOC113788269	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2809912	NM_006129.5(BMP1):c.1518C>T (p.Ile506=)	BMP1, LOC113788269	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2807990	NM_006129.5(BMP1):c.1410C>G (p.Gly470=)	BMP1, LOC113788269	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2807837	NM_006129.5(BMP1):c.78C>G (p.Ala26=)	BMP1, LOC129999976	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2807564	NM_006129.5(BMP1):c.6C>G (p.Pro2=)	BMP1, LOC129999976	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2806831	NM_006129.5(BMP1):c.1444-13C>G	BMP1, LOC113788269	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2800827	NM_006129.5(BMP1):c.114G>A (p.Ser38=)	BMP1, LOC129999976	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2796453	NM_006129.5(BMP1):c.1765+8C>T	BMP1, LOC113788269	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2795023	NM_006129.5(BMP1):c.148+16C>A	BMP1, LOC129999976	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2792454	NM_006129.5(BMP1):c.1444-13C>A	BMP1, LOC113788269	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2785417	NM_006129.5(BMP1):c.1476T>C (p.Tyr492=)	BMP1, LOC113788269	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2785279	NM_006129.5(BMP1):c.1444-9G>C	BMP1, LOC113788269	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2783499	NM_006129.5(BMP1):c.1444-18T>C	BMP1, LOC113788269	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2779669	NM_006129.5(BMP1):c.78C>T (p.Ala26=)	BMP1, LOC129999976	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2779380	NM_006129.5(BMP1):c.148+17C>A	BMP1, LOC129999976	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2779283	NM_006129.5(BMP1):c.96G>T (p.Leu32=)	BMP1, LOC129999976	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2778300	NM_006129.5(BMP1):c.1444-10C>G	BMP1, LOC113788269	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2777138	NM_006129.5(BMP1):c.1518C>A (p.Ile506=)	BMP1, LOC113788269	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2763741	NM_006129.5(BMP1):c.1725C>T (p.Asp575=)	BMP1, LOC113788269	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2763678	NM_006129.5(BMP1):c.1765+10C>T	BMP1, LOC113788269	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2763661	NM_006129.5(BMP1):c.1444-17G>T	BMP1, LOC113788269	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2763412	NM_006129.5(BMP1):c.1332C>A (p.Gly444=)	BMP1, LOC113788269	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2759080	NM_006129.5(BMP1):c.1765+19C>A	BMP1, LOC113788269	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2758473	NM_006129.5(BMP1):c.1444-7C>A	BMP1, LOC113788269	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2756571	NM_006129.5(BMP1):c.1701G>A (p.Leu567=)	BMP1, LOC113788269	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2755299	NM_006129.5(BMP1):c.51G>T (p.Pro17=)	BMP1, LOC129999976	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2748987	NM_006129.5(BMP1):c.1644G>A (p.Val548=)	BMP1, LOC113788269	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2744973	NM_006129.5(BMP1):c.1641G>A (p.Glu547=)	BMP1, LOC113788269	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2735698	NM_006129.5(BMP1):c.1639+7C>G	BMP1, LOC113788269	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2728799	NM_006129.5(BMP1):c.1311T>C (p.Gly437=)	BMP1, LOC113788269	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2727222	NM_006129.5(BMP1):c.1444-15A>T	BMP1, LOC113788269	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2718396	NM_006129.5(BMP1):c.1596C>T (p.Asp532=)	BMP1, LOC113788269	Single nucleotide variant (non-coding transcript variant +1 more)	not provided	GLikely benign
Select item 2717504	NM_006129.5(BMP1):c.1527C>T (p.Tyr509=)	BMP1, LOC113788269	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2716445	NM_006129.5(BMP1):c.1653C>T (p.Cys551=)	BMP1, LOC113788269	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2708649	NM_006129.5(BMP1):c.1444-14G>A	BMP1, LOC113788269	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2707590	NM_006129.5(BMP1):c.1444-9G>T	BMP1, LOC113788269	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2700600	NM_006129.5(BMP1):c.96G>A (p.Leu32=)	BMP1, LOC129999976	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2613279	NM_006129.5(BMP1):c.1702G>A (p.Gly568Ser)	BMP1, LOC113788269 (G568S)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance

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