HENMT1[gene] and "single gene"[properties] - ClinVar

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Items: 29

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2539886	NM_001102592.2(HENMT1):c.1154A>C (p.Asn385Thr)	HENMT1 (N385T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2349643	NM_001102592.2(HENMT1):c.1151G>A (p.Arg384His)	HENMT1 (R384H)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3284011	NM_001102592.2(HENMT1):c.1150C>T (p.Arg384Cys)	HENMT1 (R384C)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2268796	NM_001102592.2(HENMT1):c.1114C>G (p.Leu372Val)	HENMT1 (L372V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 780253	NM_001102592.2(HENMT1):c.1072A>G (p.Asn358Asp)	HENMT1 (N358D)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 2210078	NM_001102592.2(HENMT1):c.1061G>A (p.Arg354His)	HENMT1 (R354H)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3105239	NM_001102592.2(HENMT1):c.1021G>A (p.Val341Ile)	HENMT1 (V341I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2609548	NM_001102592.2(HENMT1):c.977T>C (p.Ile326Thr)	HENMT1 (I326T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2491451	NM_001102592.2(HENMT1):c.721C>G (p.Leu241Val)	HENMT1 (L241V)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 727198	NM_001102592.2(HENMT1):c.689G>A (p.Arg230Gln)	HENMT1 (R230Q)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 2529966	NM_001102592.2(HENMT1):c.667T>C (p.Cys223Arg)	HENMT1 (C223R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3105242	NM_001102592.2(HENMT1):c.637C>A (p.Pro213Thr)	HENMT1 (P213T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2638963	NM_001102592.2(HENMT1):c.630C>T (p.Val210=)	HENMT1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 3284012	NM_001102592.2(HENMT1):c.616G>A (p.Glu206Lys)	HENMT1 (E206K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2311539	NM_001102592.2(HENMT1):c.589G>T (p.Val197Leu)	HENMT1 (V197L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2235476	NM_001102592.2(HENMT1):c.542A>G (p.His181Arg)	HENMT1 (H181R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1328956	NM_001102592.2(HENMT1):c.456C>G (p.Tyr152Ter)	HENMT1 (Y152*)	Single nucleotide variant (nonsense)	Azoospermia	GPathogenic
Select item 2411366	NM_001102592.2(HENMT1):c.400A>T (p.Ile134Leu)	HENMT1 (I134L)	Single nucleotide variant (missense variant)	Male infertility +1 more	GUncertain significance
Select item 2467058	NM_001102592.2(HENMT1):c.386C>T (p.Thr129Met)	HENMT1 (T129M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3105241	NM_001102592.2(HENMT1):c.371G>A (p.Gly124Glu)	HENMT1 (G124E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2220832	NM_001102592.2(HENMT1):c.366G>T (p.Leu122Phe)	HENMT1 (L122F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2456035	NM_001102592.2(HENMT1):c.338G>C (p.Gly113Ala)	HENMT1 (G113A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3105240	NM_001102592.2(HENMT1):c.269C>T (p.Ser90Leu)	HENMT1 (S90L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1684794	NM_001102592.2(HENMT1):c.253C>T (p.Arg85Ter)	HENMT1 (R85*)	Single nucleotide variant (nonsense)	not specified	GUncertain significance
Select item 1328955	NM_001102592.2(HENMT1):c.226G>A (p.Gly76Arg)	HENMT1 (G76R)	Single nucleotide variant (missense variant)	Azoospermia	GPathogenic
Select item 2306244	NM_001102592.2(HENMT1):c.209G>A (p.Cys70Tyr)	HENMT1 (C70Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2546305	NM_001102592.2(HENMT1):c.151G>A (p.Val51Ile)	HENMT1 (V51I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 787209	NM_001102592.2(HENMT1):c.114C>T (p.Phe38=)	HENMT1	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 2604359	NM_001102592.2(HENMT1):c.112T>C (p.Phe38Leu)	HENMT1 (F38L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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Items: 29