"Ambry Genetics"[submitter] AND "DUSP13B"[gene] - ClinVar

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Items: 25

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3235488	NM_001363514.2(DUSP13B):c.992C>T (p.Thr331Met)	DUSP13B (T195M +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2295110	NM_001363514.2(DUSP13B):c.985C>T (p.Arg329Trp)	DUSP13B (R193W +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2271419	NM_001363514.2(DUSP13B):c.958C>G (p.Leu320Val)	DUSP13B (L234V +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3235487	NM_001363514.2(DUSP13B):c.953G>A (p.Arg318Gln)	DUSP13B (R182Q +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2204198	NM_001363514.2(DUSP13B):c.952C>T (p.Arg318Trp)	DUSP13B (R318W +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3235486	NM_001363514.2(DUSP13B):c.932G>T (p.Cys311Phe)	DUSP13B (C175F +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2334196	NM_001363514.2(DUSP13B):c.923G>A (p.Arg308His)	DUSP13B (R172H +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3235484	NM_001363514.2(DUSP13B):c.860C>A (p.Ala287Asp)	DUSP13B (A151D +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3274046	NM_001363514.2(DUSP13B):c.839G>A (p.Arg280His)	DUSP13B (R144H +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3235483	NM_001363514.2(DUSP13B):c.838C>T (p.Arg280Cys)	DUSP13B (R144C +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2304012	NM_001363514.2(DUSP13B):c.826A>T (p.Met276Leu)	DUSP13B (M276L +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3235482	NM_001363514.2(DUSP13B):c.806G>A (p.Arg269His)	DUSP13B (R133H +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3235481	NM_001363514.2(DUSP13B):c.805C>T (p.Arg269Cys)	DUSP13B (R133C +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2305254	NM_001363514.2(DUSP13B):c.793G>A (p.Val265Ile)	DUSP13B (V129I +3 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2292646	NM_001363514.2(DUSP13B):c.785C>G (p.Ala262Gly)	DUSP13B (A126G +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2361596	NM_001363514.2(DUSP13B):c.770G>A (p.Arg257Gln)	DUSP13B (R121Q +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3235480	NM_001363514.2(DUSP13B):c.767C>A (p.Ala256Asp)	DUSP13B (A120D +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3235479	NM_001363514.2(DUSP13B):c.654G>C (p.Lys218Asn)	DUSP13B (K132N +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2292009	NM_001363514.2(DUSP13B):c.628C>G (p.His210Asp)	DUSP13B (H74D +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3235478	NM_001363514.2(DUSP13B):c.615G>T (p.Gln205His)	DUSP13B (Q119H +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3235477	NM_001363514.2(DUSP13B):c.595G>C (p.Asp199His)	DUSP13B (D113H +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2347946	NM_001363514.2(DUSP13B):c.521G>A (p.Arg174His)	DUSP13B (R88H +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2345348	NM_001363514.2(DUSP13B):c.482C>A (p.Pro161Gln)	DUSP13B (P25Q +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2215657	NM_001363514.2(DUSP13B):c.482C>T (p.Pro161Leu)	DUSP13B (P118L +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3235476	NM_001363514.2(DUSP13B):c.437G>A (p.Arg146Gln)	DUSP13B (R103Q +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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Items: 25