H1-10[gene] and "single gene"[properties] - ClinVar - NCBI

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Items: 14

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3103472	NM_006026.4(H1-10):c.572C>T (p.Ala191Val)	H1-10 (A191V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3103470	NM_006026.4(H1-10):c.461C>G (p.Ser154Cys)	H1-10 (S154C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2476914	NM_006026.4(H1-10):c.455C>T (p.Ala152Val)	H1-10 (A152V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3103469	NM_006026.4(H1-10):c.445C>T (p.Pro149Ser)	H1-10 (P149S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3103468	NM_006026.4(H1-10):c.418A>C (p.Thr140Pro)	H1-10 (T140P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2615508	NM_006026.4(H1-10):c.221C>G (p.Ala74Gly)	H1-10 (A74G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3103464	NM_006026.4(H1-10):c.172A>G (p.Arg58Gly)	H1-10 (R58G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3283249	NM_006026.4(H1-10):c.169C>T (p.Arg57Cys)	H1-10 (R57C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3103462	NM_006026.4(H1-10):c.126G>C (p.Lys42Asn)	H1-10 (K42N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3103461	NM_006026.4(H1-10):c.107G>A (p.Arg36Lys)	H1-10 (R36K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2520365	NM_006026.4(H1-10):c.97T>C (p.Ser33Pro)	H1-10 (S33P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3103471	NM_006026.4(H1-10):c.49A>C (p.Met17Leu)	H1-10 (M17L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2612237	NM_006026.4(H1-10):c.23C>T (p.Ala8Val)	H1-10 (A8V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3103463	NM_006026.4(H1-10):c.13C>T (p.Leu5Phe)	H1-10 (L5F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance