"Ambry Genetics"[submitter] AND "ARNT2"[gene] - ClinVar

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Items: 32

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2331005	NM_014862.4(ARNT2):c.8C>A (p.Thr3Asn)	ARNT2 (T3N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1971148	NM_014862.4(ARNT2):c.62C>T (p.Thr21Met)	ARNT2 (T21M)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 2613516	NM_014862.4(ARNT2):c.91G>A (p.Gly31Arg)	ARNT2 (G31R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2255269	NM_014862.4(ARNT2):c.97G>A (p.Val33Met)	ARNT2 (V33M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2454686	NM_014862.4(ARNT2):c.125G>C (p.Arg42Pro)	ARNT2 (R42P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2474215	NM_014862.4(ARNT2):c.238A>G (p.Thr80Ala)	ARNT2 (T80A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3129740	NM_014862.4(ARNT2):c.368C>A (p.Ser123Tyr)	ARNT2 (S123Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2623961	NM_014862.4(ARNT2):c.463G>C (p.Ala155Pro)	ARNT2 (A155P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2270345	NM_014862.4(ARNT2):c.499G>A (p.Val167Ile)	ARNT2 (V167I)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 2233774	NM_014862.4(ARNT2):c.554A>G (p.Glu185Gly)	ARNT2 (E185G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3129741	NM_014862.4(ARNT2):c.573C>G (p.Asp191Glu)	ARNT2 (D191E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3129742	NM_014862.4(ARNT2):c.729T>G (p.Cys243Trp)	ARNT2 (C243W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3129743	NM_014862.4(ARNT2):c.739C>G (p.Pro247Ala)	ARNT2 (P247A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2079535	NM_014862.4(ARNT2):c.785G>A (p.Arg262Lys)	ARNT2 (R262K)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 801401	NM_014862.4(ARNT2):c.1000C>T (p.Pro334Ser)	ARNT2 (P334S)	Single nucleotide variant (missense variant)	not provided +2 more	GUncertain significance
Select item 2616875	NM_014862.4(ARNT2):c.1072A>G (p.Ile358Val)	ARNT2 (I358V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2336935	NM_014862.4(ARNT2):c.1148G>A (p.Arg383His)	ARNT2, LOC101929586 (R383H)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2557515	NM_014862.4(ARNT2):c.1223G>A (p.Arg408Gln)	ARNT2 (R408Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2209698	NM_014862.4(ARNT2):c.1310A>G (p.Asn437Ser)	ARNT2 (N437S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3315909	NM_014862.4(ARNT2):c.1363G>A (p.Gly455Arg)	ARNT2 (G455R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1341858	NM_014862.4(ARNT2):c.1414G>A (p.Gly472Ser)	ARNT2 (G472S)	Single nucleotide variant (missense variant)	Webb-Dattani syndrome +2 more	GUncertain significance
Select item 3129736	NM_014862.4(ARNT2):c.1429G>C (p.Gly477Arg)	ARNT2 (G477R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2222717	NM_014862.4(ARNT2):c.1441G>C (p.Glu481Gln)	ARNT2 (E481Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2283270	NM_014862.4(ARNT2):c.1481G>A (p.Arg494Gln)	ARNT2 (R494Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3129737	NM_014862.4(ARNT2):c.1544C>T (p.Ala515Val)	ARNT2 (A515V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2551082	NM_014862.4(ARNT2):c.1556A>G (p.Gln519Arg)	ARNT2 (Q519R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2189028	NM_014862.4(ARNT2):c.1636G>A (p.Gly546Arg)	ARNT2 (G546R)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 3129738	NM_014862.4(ARNT2):c.1694G>A (p.Arg565Gln)	ARNT2 (R565Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2525289	NM_014862.4(ARNT2):c.1736C>T (p.Pro579Leu)	ARNT2 (P579L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2384549	NM_014862.4(ARNT2):c.1820C>T (p.Pro607Leu)	ARNT2 (P607L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2305010	NM_014862.4(ARNT2):c.1982A>G (p.Gln661Arg)	ARNT2 (Q661R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3129739	NM_014862.4(ARNT2):c.2008G>A (p.Gly670Ser)	ARNT2 (G670S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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Items: 32