Related gene-specific medical variations for Gene (Select 51281) - ClinVar - NCBI

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Items: 18

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3086309	NM_001370465.2(DUSP28):c.34G>A (p.Ala12Thr)	ANKMY1, DUSP28 (A12T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3086307	NM_001370465.2(DUSP28):c.337G>C (p.Val113Leu)	ANKMY1, DUSP28 +1 more (V113L)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3086306	NM_001370465.2(DUSP28):c.214G>A (p.Asp72Asn)	ANKMY1, DUSP28 (S18L +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3086305	NM_001370465.2(DUSP28):c.122C>G (p.Ala41Gly)	ANKMY1, DUSP28 +1 more (A49P +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2613809	NM_001370465.2(DUSP28):c.341G>A (p.Cys114Tyr)	ANKMY1, DUSP28 +1 more (C114Y)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2597829	NM_001370465.2(DUSP28):c.208G>A (p.Val70Met)	ANKMY1, DUSP28 (V70M +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2591111	NM_001370465.2(DUSP28):c.329C>T (p.Ser110Leu)	ANKMY1, DUSP28 +1 more (S110L)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2547639	NM_001370465.2(DUSP28):c.347C>T (p.Ala116Val)	ANKMY1, DUSP28 +1 more (A116V)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2547358	NM_001370465.2(DUSP28):c.70C>A (p.Pro24Thr)	ANKMY1, DUSP28 (P24T +1 more)	Single nucleotide variant (missense variant +3 more)	not specified	GUncertain significance
Select item 2536054	NM_001370465.2(DUSP28):c.236T>C (p.Leu79Pro)	ANKMY1, DUSP28 (L79P +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2481177	NM_001370465.2(DUSP28):c.356T>A (p.Met119Lys)	ANKMY1, DUSP28 +1 more (M1L +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2463718	NM_001370465.2(DUSP28):c.359G>C (p.Arg120Pro)	ANKMY1, DUSP28 +1 more (R120P)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2395174	NM_001370465.2(DUSP28):c.163C>A (p.Gln55Lys)	ANKMY1, DUSP28 (C35F +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2386645	NM_001370465.2(DUSP28):c.38C>T (p.Ser13Leu)	ANKMY1, DUSP28 (S13L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2357469	NM_001370465.2(DUSP28):c.19G>A (p.Gly7Arg)	ANKMY1, DUSP28 (G7R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2316562	NM_001370465.2(DUSP28):c.53C>A (p.Pro18Gln)	ANKMY1, DUSP28 (P18Q +1 more)	Single nucleotide variant (missense variant +3 more)	not specified	GUncertain significance
Select item 2256133	NM_001370465.2(DUSP28):c.181C>T (p.Pro61Ser)	ANKMY1, DUSP28 (G29D +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2208451	NM_001370465.2(DUSP28):c.359G>A (p.Arg120Gln)	ANKMY1, DUSP28 +1 more (R120Q)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance