Related gene-specific medical variations for Gene (Select 138639) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3311373	NM_001253829.2(PTPDC1):c.107A>G (p.Gln36Arg)	LOC124310590, PTPDC1 (Q36R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3149051	NM_001253829.2(PTPDC1):c.70C>T (p.Arg24Trp)	LOC124310590, PTPDC1 (R24W)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3149050	NM_001253829.2(PTPDC1):c.5A>G (p.Gln2Arg)	LOC124310590, PTPDC1 (Q2R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3149043	NM_001253829.2(PTPDC1):c.150G>C (p.Lys50Asn)	LOC124310590, PTPDC1 (K50N)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2492256	NM_001253829.2(PTPDC1):c.125G>A (p.Gly42Asp)	LOC124310590, PTPDC1 (G42D)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2333966	NM_001253829.2(PTPDC1):c.146C>T (p.Thr49Met)	LOC124310590, PTPDC1 (T49M)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2306925	NM_001253829.2(PTPDC1):c.136G>A (p.Gly46Ser)	LOC124310590, PTPDC1 (G46S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance

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