CARM1[gene] and "single gene"[properties] - ClinVar - NCBI

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Items: 17

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2248989	NM_199141.2(CARM1):c.20C>T (p.Ala7Val)	CARM1 (A7V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3137374	NM_199141.2(CARM1):c.116C>G (p.Thr39Ser)	CARM1 (T39S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2521949	NM_199141.2(CARM1):c.164C>A (p.Ala55Glu)	CARM1 (A55E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2616274	NM_199141.2(CARM1):c.319G>A (p.Val107Ile)	CARM1 (V107I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 992650	NM_199141.2(CARM1):c.362A>T (p.Tyr121Phe)	CARM1 (Y121F +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2239825	NM_199141.2(CARM1):c.382C>T (p.Arg128Trp)	CARM1 (R128W +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3137379	NM_199141.2(CARM1):c.401G>A (p.Arg134Gln)	CARM1 (R134Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3252067	NM_199141.2(CARM1):c.421A>G (p.Thr141Ala)	CARM1 (T106A +1 more)	Single nucleotide variant (missense variant)	Neurodevelopmental disorder	GUncertain significance
Select item 3137380	NM_199141.2(CARM1):c.439G>T (p.Val147Leu)	CARM1 (V112L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2363725	NM_199141.2(CARM1):c.604G>T (p.Ala202Ser)	CARM1 (A202S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 783826	NM_199141.2(CARM1):c.678G>A (p.Val226=)	CARM1	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 3137376	NM_199141.2(CARM1):c.1281C>G (p.Phe427Leu)	CARM1 (F392L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3263323	NM_199141.2(CARM1):c.1282G>A (p.Ala428Thr)	CARM1 (A393T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2315008	NM_199141.2(CARM1):c.1378G>A (p.Gly460Ser)	CARM1 (G425S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3263325	NM_199141.2(CARM1):c.1609C>G (p.Pro537Ala)	CARM1 (P502A +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3137377	NM_199141.2(CARM1):c.1721C>T (p.Thr574Met)	CARM1 (T516M +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 777443	NM_199141.2(CARM1):c.1722G>A (p.Thr574=)	CARM1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign