Related gene-specific medical variations for Gene (Select 388335) - ClinVar - NCBI

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Items: 5

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3179182	NM_001004313.3(TMEM220):c.31G>A (p.Gly11Arg)	TMEM220, TMEM220-AS1 (G11R)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2555712	NM_001004313.3(TMEM220):c.59C>A (p.Ala20Glu)	TMEM220, TMEM220-AS1 (A20E)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2296614	NM_001004313.3(TMEM220):c.62C>T (p.Ala21Val)	TMEM220, TMEM220-AS1 (A21V)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2234393	NM_001004313.3(TMEM220):c.37A>T (p.Met13Leu)	TMEM220, TMEM220-AS1 (M13L)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2206610	NM_001004313.3(TMEM220):c.10G>A (p.Ala4Thr)	TMEM220, TMEM220-AS1 (A4T)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance

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