Related gene-specific medical variations for Gene (Select 11099) - ClinVar - NCBI

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Items: 10

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3149170	NM_007039.4(PTPN21):c.3302A>G (p.Asn1101Ser)	PTPN21, SPATA7 (N1101S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3149169	NM_007039.4(PTPN21):c.3004G>A (p.Gly1002Ser)	PTPN21, SPATA7 (G1002S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2644435	NM_007039.4(PTPN21):c.3051G>A (p.Arg1017=)	PTPN21, SPATA7	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2600482	NM_007039.4(PTPN21):c.3403G>C (p.Asp1135His)	PTPN21, SPATA7 (D1135H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2542104	NM_007039.4(PTPN21):c.3487G>A (p.Val1163Ile)	PTPN21, SPATA7 (V1163I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2379650	NM_007039.4(PTPN21):c.3299C>T (p.Pro1100Leu)	PTPN21, SPATA7 (P1100L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2311165	NM_007039.4(PTPN21):c.3430A>G (p.Arg1144Gly)	PTPN21, SPATA7 (R1144G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2267601	NM_007039.4(PTPN21):c.3268C>T (p.His1090Tyr)	PTPN21, SPATA7 (H1090Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 768670	NM_007039.4(PTPN21):c.3296G>A (p.Ser1099Asn)	PTPN21, SPATA7 (S1099N)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 161654	NM_007039.4(PTPN21):c.94A>C (p.Asn32His)	PTPN21 (N32H)	Single nucleotide variant (missense variant)	Malignant tumor of prostate	GUncertain significance