Related gene-specific medical variations for Gene (Select 84336) - ClinVar - NCBI

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Items: 11

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3178390	NM_032376.4(TMEM101):c.43A>T (p.Ile15Phe)	LOC126862572, TMEM101 (I15F)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3178388	NM_032376.4(TMEM101):c.16G>C (p.Gly6Arg)	LOC126862572, TMEM101 (G6R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3178387	NM_032376.4(TMEM101):c.12G>C (p.Lys4Asn)	LOC126862572, TMEM101 (K4N)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2547614	NM_032376.4(TMEM101):c.65T>C (p.Leu22Pro)	LOC126862572, TMEM101 (L22P)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2482776	NM_032376.4(TMEM101):c.245C>T (p.Ala82Val)	LOC126862572, TMEM101 (A24V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2475134	NM_032376.4(TMEM101):c.16G>A (p.Gly6Ser)	LOC126862572, TMEM101 (G6S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2408479	NM_032376.4(TMEM101):c.77G>A (p.Cys26Tyr)	LOC126862572, TMEM101 (C26Y)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2356368	NM_032376.4(TMEM101):c.274G>A (p.Ala92Thr)	LOC126862572, TMEM101 (A34T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2295082	NM_032376.4(TMEM101):c.284T>A (p.Ile95Asn)	LOC126862572, TMEM101 (I95N +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2253665	NM_032376.4(TMEM101):c.88G>T (p.Gly30Cys)	LOC126862572, TMEM101 (G30C)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 774518	NM_032376.4(TMEM101):c.54G>A (p.Leu18=)	LOC126862572, TMEM101	Single nucleotide variant (synonymous variant +1 more)	not provided	GBenign