Related gene-specific medical variations for Gene (Select 169200) - ClinVar

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Links from Gene

Items: 21

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3327166	NM_001008495.4(TMEM64):c.625G>T (p.Ala209Ser)	LOC130000720, TMEM64 (A209S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3327165	NM_001008495.4(TMEM64):c.212A>G (p.Glu71Gly)	LOC130000721, TMEM64 (E71G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3327164	NM_001008495.4(TMEM64):c.220G>C (p.Gly74Arg)	LOC130000721, TMEM64 (G74R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3327163	NM_001008495.4(TMEM64):c.76G>A (p.Glu26Lys)	LOC130000721, TMEM64 (E26K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3327162	NM_001008495.4(TMEM64):c.748G>A (p.Ala250Thr)	LOC130000720, TMEM64 (A250T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3179610	NM_001008495.4(TMEM64):c.715G>A (p.Glu239Lys)	LOC130000720, TMEM64 (E239K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3179609	NM_001008495.4(TMEM64):c.596T>C (p.Met199Thr)	LOC130000720, TMEM64 (M199T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3179608	NM_001008495.4(TMEM64):c.55G>T (p.Ala19Ser)	LOC130000721, TMEM64 (A19S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3179606	NM_001008495.4(TMEM64):c.340C>T (p.Leu114Phe)	LOC130000721, TMEM64 (L114F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3179605	NM_001008495.4(TMEM64):c.152G>T (p.Gly51Val)	LOC130000721, TMEM64 (G51V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3179604	NM_001008495.4(TMEM64):c.151G>T (p.Gly51Trp)	LOC130000721, TMEM64 (G51W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3179603	NM_001008495.4(TMEM64):c.142C>T (p.Arg48Cys)	LOC130000721, TMEM64 (R48C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2538932	NM_001008495.4(TMEM64):c.602G>A (p.Gly201Asp)	LOC130000720, TMEM64 (G201D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2535994	NM_001008495.4(TMEM64):c.37C>A (p.Pro13Thr)	LOC130000721, TMEM64 (P13T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2528752	NM_001008495.4(TMEM64):c.86C>T (p.Ala29Val)	LOC130000721, TMEM64 (A29V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2515950	NM_001008495.4(TMEM64):c.205T>C (p.Tyr69His)	LOC130000721, TMEM64 (Y69H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2515602	NM_001008495.4(TMEM64):c.128C>A (p.Ala43Glu)	LOC130000721, TMEM64 (A43E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2493050	NM_001008495.4(TMEM64):c.130G>C (p.Asp44His)	LOC130000721, TMEM64 (D44H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2364500	NM_001008495.4(TMEM64):c.151G>A (p.Gly51Arg)	LOC130000721, TMEM64 (G51R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2290667	NM_001008495.4(TMEM64):c.8G>A (p.Ser3Asn)	LOC130000721, TMEM64 (S3N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2243816	NM_001008495.4(TMEM64):c.593T>C (p.Met198Thr)	LOC130000720, TMEM64 (M198T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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Links from Gene

Items: 21