Related gene-specific medical variations for Gene (Select 7803) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3149033	NM_003463.5(PTP4A1):c.92A>G (p.Asn31Ser)	LOC128125822, PTP4A1 (N15S +1 more)	Single nucleotide variant (3 prime UTR variant +2 more)	not specified	GUncertain significance
Select item 3149032	NM_003463.5(PTP4A1):c.278G>A (p.Arg93His)	LOC128125822, PTP4A1 (R77H +2 more)	Single nucleotide variant (3 prime UTR variant +2 more)	not specified	GUncertain significance
Select item 2411613	NM_003463.5(PTP4A1):c.413G>A (p.Arg138His)	LOC128125822, PTP4A1 (R122H +3 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2335960	NM_003463.5(PTP4A1):c.237G>C (p.Gln79His)	LOC128125822, PTP4A1 (Q63H +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 716894	NM_003463.5(PTP4A1):c.439C>T (p.Leu147=)	LOC128125822, PTP4A1	Single nucleotide variant (synonymous variant +2 more)	not provided	GBenign
Select item 716893	NM_003463.5(PTP4A1):c.411G>T (p.Arg137=)	LOC128125822, PTP4A1 (A152S +1 more)	Single nucleotide variant (synonymous variant +2 more)	not provided	GBenign

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