"Ambry Genetics"[submitter] AND "ARMT1"[gene] - ClinVar

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Items: 26

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2558252	NM_024573.3(ARMT1):c.175A>G (p.Ile59Val)	ARMT1 (I59V)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2402421	NM_024573.3(ARMT1):c.225T>A (p.Phe75Leu)	ARMT1 (F75L)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2299918	NM_024573.3(ARMT1):c.256G>A (p.Asp86Asn)	ARMT1 (D86N)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2602831	NM_024573.3(ARMT1):c.259A>G (p.Ile87Val)	ARMT1 (I87V)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 3129726	NM_024573.3(ARMT1):c.304A>C (p.Ser102Arg)	ARMT1 (S102R)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2242571	NM_024573.3(ARMT1):c.335C>T (p.Pro112Leu)	ARMT1 (P112L)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 3129728	NM_024573.3(ARMT1):c.339G>T (p.Trp113Cys)	ARMT1 (W113C)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2216504	NM_024573.3(ARMT1):c.373C>A (p.His125Asn)	ARMT1 (H6N +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2288966	NM_024573.3(ARMT1):c.418T>C (p.Phe140Leu)	ARMT1 (F21L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3129729	NM_024573.3(ARMT1):c.602G>A (p.Gly201Glu)	ARMT1 (G201E +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3129730	NM_024573.3(ARMT1):c.781A>G (p.Thr261Ala)	ARMT1 (T261A +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2352697	NM_024573.3(ARMT1):c.853A>G (p.Ile285Val)	ARMT1 (I166V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3129731	NM_024573.3(ARMT1):c.877A>G (p.Thr293Ala)	ARMT1 (T174A +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2462108	NM_024573.3(ARMT1):c.880A>G (p.Ile294Val)	ARMT1 (I175V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2301060	NM_024573.3(ARMT1):c.918C>A (p.His306Gln)	ARMT1 (H187Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2521984	NM_024573.3(ARMT1):c.936G>A (p.Met312Ile)	ARMT1 (M193I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2539413	NM_024573.3(ARMT1):c.988T>A (p.Tyr330Asn)	ARMT1 (Y211N +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3129723	NM_024573.3(ARMT1):c.1019A>G (p.His340Arg)	ARMT1 (H221R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2619904	NM_024573.3(ARMT1):c.1021G>A (p.Glu341Lys)	ARMT1 (E222K +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3129724	NM_024573.3(ARMT1):c.1023G>T (p.Glu341Asp)	ARMT1 (E341D +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2277552	NM_024573.3(ARMT1):c.1031C>G (p.Ala344Gly)	ARMT1 (A225G +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2412249	NM_024573.3(ARMT1):c.1033A>G (p.Met345Val)	ARMT1 (M345V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2354636	NM_024573.3(ARMT1):c.1057T>C (p.Tyr353His)	ARMT1 (Y234H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2404629	NM_024573.3(ARMT1):c.1084A>G (p.Ile362Val)	ARMT1 (I243V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2558049	NM_024573.3(ARMT1):c.1094A>G (p.Lys365Arg)	ARMT1 (K365R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3129725	NM_024573.3(ARMT1):c.1282A>G (p.Thr428Ala)	ARMT1 (T428A +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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Items: 26