ClinVar Miner

List of variants in gene PTPN14 studied for benign neoplasm

Included ClinVar conditions (127):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 21
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HGVS dbSNP gnomAD frequency
NM_005401.5(PTPN14):c.-26G>A rs10864100 0.83031
NM_005401.5(PTPN14):c.2688+26C>T rs3013451 0.82386
NM_005401.5(PTPN14):c.978A>G (p.Arg326=) rs7550799 0.82382
NM_005401.5(PTPN14):c.3252A>G (p.Glu1084=) rs1135352 0.81332
NM_005401.5(PTPN14):c.758+5T>G rs11580603 0.37880
NM_005401.5(PTPN14):c.*26G>A rs2291831 0.15689
NM_005401.5(PTPN14):c.*6320C>T
NM_005401.5(PTPN14):c.-154-22749A>G
NM_005401.5(PTPN14):c.-154-42562G>A
NM_005401.5(PTPN14):c.1574C>T (p.Pro525Leu)
NM_005401.5(PTPN14):c.1583C>T (p.Pro528Leu)
NM_005401.5(PTPN14):c.2164C>T (p.Pro722Ser)
NM_005401.5(PTPN14):c.2216C>T (p.Ala739Val)
NM_005401.5(PTPN14):c.2596A>G (p.Met866Val)
NM_005401.5(PTPN14):c.3500T>C (p.Ile1167Thr)
NM_005401.5(PTPN14):c.401_402insTT (p.Leu135fs) rs1558092113
NM_005401.5(PTPN14):c.456C>G (p.Asp152Glu)
NM_005401.5(PTPN14):c.581+60_669+877del
NM_005401.5(PTPN14):c.679G>T (p.Gly227Ter)
NM_005401.5(PTPN14):c.715A>T (p.Ile239Phe)
NM_005401.5(PTPN14):c.929+24del rs11322819

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