C4225367[trait identifier] AND "Baylor Genetics"[submitter] - ClinVar

Warning: The NCBI web site requires JavaScript to function. more...

Search results

Items: 38

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 847394	NM_005055.5(RAPSN):c.1116GAA[1] (p.Lys373del)	RAPSN (K314del +1 more)	Microsatellite (inframe_deletion)	Fetal akinesia deformation sequence 2 +4 more	GPathogenic
Select item 632161	NM_005055.5(RAPSN):c.1029_1045del (p.Glu344fs)	RAPSN (E285fs +1 more)	Deletion (frameshift variant)	RAPSN-related disorder +3 more	GConflicting classifications of pathogenicity
Select item 664620	NM_005055.5(RAPSN):c.997G>T (p.Glu333Ter)	RAPSN (E333* +1 more)	Single nucleotide variant (nonsense)	Fetal akinesia deformation sequence 2 +2 more	GPathogenic
Select item 2137088	NM_005055.5(RAPSN):c.990_993del (p.His329_Cys330insTer)	RAPSN	Deletion (nonsense)	Congenital myasthenic syndrome 11 +2 more	GPathogenic
Select item 1481997	NM_005055.5(RAPSN):c.966+1_966+2delinsAG	RAPSN	Indel (intron variant +1 more)	Fetal akinesia deformation sequence 2 +2 more	GPathogenic/Likely pathogenic
Select item 2678228	NM_005055.5(RAPSN):c.913-1G>C	RAPSN	Single nucleotide variant (intron variant +1 more)	Congenital myasthenic syndrome 11 +2 more	GLikely pathogenic
Select item 689779	NM_005055.5(RAPSN):c.872G>A (p.Gly291Asp)	RAPSN (G291D)	Single nucleotide variant (missense variant +1 more)	Fetal akinesia deformation sequence 2 +3 more	GConflicting classifications of pathogenicity
Select item 8052	NM_005055.5(RAPSN):c.848T>C (p.Leu283Pro)	RAPSN (L283P)	Single nucleotide variant (missense variant +1 more)	Congenital myasthenic syndrome 11 +5 more	GConflicting classifications of pathogenicity
Select item 197248	NM_005055.5(RAPSN):c.737C>T (p.Ala246Val)	RAPSN (A246V)	Single nucleotide variant (missense variant)	Fetal akinesia deformation sequence 2 +3 more	GPathogenic/Likely pathogenic
Select item 2057011	NM_005055.5(RAPSN):c.724C>T (p.Arg242Trp)	RAPSN (R242W)	Single nucleotide variant (missense variant)	Fetal akinesia deformation sequence 1 +2 more	GConflicting classifications of pathogenicity
Select item 1416981	NM_005055.5(RAPSN):c.712C>T (p.Gln238Ter)	RAPSN (Q238*)	Single nucleotide variant (nonsense)	Fetal akinesia deformation sequence 2 +2 more	GPathogenic
Select item 1072315	NM_005055.5(RAPSN):c.599G>A (p.Trp200Ter)	RAPSN (W200*)	Single nucleotide variant (nonsense)	Fetal akinesia deformation sequence 2 +2 more	GPathogenic/Likely pathogenic
Select item 1067929	NM_005055.5(RAPSN):c.531+1G>T	RAPSN	Single nucleotide variant (splice donor variant)	Congenital myasthenic syndrome 11 +2 more	GPathogenic/Likely pathogenic
Select item 856323	NM_005055.5(RAPSN):c.493G>A (p.Val165Met)	RAPSN (V165M)	Single nucleotide variant (missense variant)	Fetal akinesia deformation sequence 1 +4 more	GPathogenic/Likely pathogenic
Select item 8054	NM_005055.5(RAPSN):c.490C>T (p.Arg164Cys)	RAPSN (R164C)	Single nucleotide variant (missense variant)	Fetal akinesia deformation sequence 2 +3 more	GPathogenic/Likely pathogenic
Select item 8056	NM_005055.5(RAPSN):c.484G>A (p.Glu162Lys)	RAPSN (E162K)	Single nucleotide variant (missense variant)	Fetal akinesia deformation sequence 2 +2 more	GPathogenic
Select item 689780	NM_005055.5(RAPSN):c.457G>A (p.Ala153Thr)	RAPSN (A153T)	Single nucleotide variant (missense variant)	Fetal akinesia deformation sequence 2 +3 more	GConflicting classifications of pathogenicity
Select item 381702	NM_005055.5(RAPSN):c.439G>A (p.Glu147Lys)	RAPSN (E147K)	Single nucleotide variant (missense variant)	not provided +4 more	GPathogenic/Likely pathogenic
Select item 859852	NM_005055.5(RAPSN):c.425C>A (p.Ala142Asp)	RAPSN (A142D)	Single nucleotide variant (missense variant)	Fetal akinesia deformation sequence 2 +4 more	GConflicting classifications of pathogenicity
Select item 1070359	NM_005055.5(RAPSN):c.418C>T (p.Gln140Ter)	RAPSN (Q140*)	Single nucleotide variant (nonsense)	Fetal akinesia deformation sequence 2 +2 more	GPathogenic/Likely pathogenic
Select item 304980	NM_005055.5(RAPSN):c.412G>A (p.Val138Ile)	RAPSN (V138I)	Single nucleotide variant (missense variant)	Congenital myasthenic syndrome 11 +2 more	GConflicting classifications of pathogenicity
Select item 476121	NM_005055.5(RAPSN):c.370C>T (p.Gln124Ter)	RAPSN (Q124*)	Single nucleotide variant (nonsense)	Fetal akinesia deformation sequence 2 +3 more	GPathogenic/Likely pathogenic
Select item 1323519	NM_005055.5(RAPSN):c.300_319del (p.His100fs)	RAPSN (H100fs)	Deletion (frameshift variant)	Fetal akinesia deformation sequence 2 +2 more	GPathogenic/Likely pathogenic
Select item 2678224	NM_005055.5(RAPSN):c.288del (p.Cys97fs)	RAPSN (C97fs)	Deletion (frameshift variant)	Congenital myasthenic syndrome 11 +2 more	GPathogenic/Likely pathogenic
Select item 1705170	NM_005055.5(RAPSN):c.280G>A (p.Glu94Lys)	RAPSN (E94K)	Single nucleotide variant (missense variant)	RAPSN-related disorder +5 more	GConflicting classifications of pathogenicity
Select item 497298	NM_005055.5(RAPSN):c.272G>T (p.Arg91Leu)	RAPSN (R91L)	Single nucleotide variant (missense variant)	Fetal akinesia deformation sequence 1 +4 more	GConflicting classifications of pathogenicity
Select item 8046	NM_005055.5(RAPSN):c.264C>A (p.Asn88Lys)	RAPSN (N88K)	Single nucleotide variant (missense variant)	Inborn genetic diseases +7 more	GPathogenic/Likely pathogenic
Select item 1455976	NM_005055.5(RAPSN):c.210del (p.Ile70fs)	RAPSN (I70fs)	Deletion (frameshift variant)	Fetal akinesia deformation sequence 2 +2 more	GPathogenic/Likely pathogenic
Select item 2678225	NM_005055.5(RAPSN):c.193-5_201del	RAPSN	Deletion (splice acceptor variant)	Congenital myasthenic syndrome 11 +2 more	GLikely pathogenic
Select item 813472	NM_005055.5(RAPSN):c.193-2A>C	RAPSN	Single nucleotide variant (splice acceptor variant)	Congenital myasthenic syndrome 11	GLikely pathogenic
Select item 2678235	NM_005055.5(RAPSN):c.192+2T>G	RAPSN	Single nucleotide variant (splice donor variant)	Congenital myasthenic syndrome 11 +2 more	GPathogenic
Select item 8055	NM_005055.5(RAPSN):c.133G>A (p.Val45Met)	RAPSN (V45M)	Single nucleotide variant (missense variant)	Congenital myasthenic syndrome 11 +3 more	GPathogenic/Likely pathogenic
Select item 802677	NM_005055.5(RAPSN):c.61C>T (p.Gln21Ter)	RAPSN (Q21*)	Single nucleotide variant (nonsense)	Fetal akinesia deformation sequence 2 +2 more	GPathogenic/Likely pathogenic
Select item 1073878	NM_005055.5(RAPSN):c.46dup (p.Leu16fs)	RAPSN (L16fs)	Duplication (frameshift variant)	Fetal akinesia deformation sequence 1 +2 more	GPathogenic
Select item 8047	NM_005055.5(RAPSN):c.41T>C (p.Leu14Pro)	RAPSN (L14P)	Single nucleotide variant (missense variant)	Fetal akinesia deformation sequence 2 +2 more	GPathogenic/Likely pathogenic
Select item 952498	NM_005055.5(RAPSN):c.11dup (p.Asp4fs)	RAPSN (D4fs)	Duplication (frameshift variant)	Fetal akinesia deformation sequence 2 +2 more	GPathogenic/Likely pathogenic
Select item 264677	NM_005055.4(RAPSN):c.-199C>G	RAPSN	Single nucleotide variant	Fetal akinesia deformation sequence 1 +3 more	GPathogenic/Likely pathogenic
Select item 8051	NM_005055.5(RAPSN):c.-210A>G	RAPSN	Single nucleotide variant	Congenital myasthenic syndrome 11 +3 more	GPathogenic/Likely pathogenic

ClinVar

Result Filters

Classification type

Germline classification

Types of conflicts

Molecular consequence

Variation type

Variation size

Variant length

Review status

Additional filters

Search results

Items: 38