Related gene-specific medical variations for Gene (Select 285193) - ClinVar

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Items: 32

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3274073	NM_001370465.2(DUSP28):c.364C>T (p.Arg122Cys)	ANKMY1, DUSP28 +1 more (R122C)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3274072	NM_001370465.2(DUSP28):c.356T>C (p.Met119Thr)	ANKMY1, DUSP28 +1 more (M119T +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3274071	NM_001370465.2(DUSP28):c.178G>A (p.Ala60Thr)	ANKMY1, DUSP28 (A30V +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3274070	NM_001370465.2(DUSP28):c.464A>C (p.Glu155Ala)	DUSP28, LOC129935975 (E155A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3274069	NM_001370465.2(DUSP28):c.229G>A (p.Asp77Asn)	ANKMY1, DUSP28 (D77N +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3086313	NM_001370465.2(DUSP28):c.488T>C (p.Leu163Pro)	DUSP28, LOC129935975 (L163P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3086312	NM_001370465.2(DUSP28):c.448C>T (p.Leu150Phe)	DUSP28, LOC129935975 (L150F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3086311	NM_001370465.2(DUSP28):c.439T>G (p.Trp147Gly)	DUSP28, LOC129935975 (W147G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3086310	NM_001370465.2(DUSP28):c.406G>T (p.Ala136Ser)	DUSP28, LOC129935975 (A136S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
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 2622502	NM_001370465.2(DUSP28):c.385G>C (p.Ala129Pro)	DUSP28, LOC106783501 (A129P)	Single nucleotide variant (missense variant)	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 2601963	NM_001370465.2(DUSP28):c.392A>G (p.Gln131Arg)	DUSP28, LOC106783501 (Q131R)	Single nucleotide variant (missense variant)	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)	DUSP28, LOC106783501 +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 2455746	NM_001370465.2(DUSP28):c.482C>T (p.Ser161Phe)	DUSP28, LOC129935975 (S161F)	Single nucleotide variant (missense variant)	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)	DUSP28, ANKMY1 (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 2248131	NM_001370465.2(DUSP28):c.515T>C (p.Leu172Ser)	DUSP28, LOC129935975 (L172S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2230723	NM_001370465.2(DUSP28):c.460G>C (p.Glu154Gln)	DUSP28, LOC129935975 (E154Q)	Single nucleotide variant (missense variant)	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

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Links from Gene

Items: 32