ClinVar Miner

List of variants in gene ATP6AP2 reported as uncertain significance for X-linked disease

Included ClinVar conditions (313):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 14
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NM_005765.3(ATP6AP2):c.1015A>G (p.Ile339Val)
NM_005765.3(ATP6AP2):c.160G>T (p.Val54Leu)
NM_005765.3(ATP6AP2):c.218G>A (p.Arg73Gln)
NM_005765.3(ATP6AP2):c.315T>G (p.Ser105Arg) rs745748841
NM_005765.3(ATP6AP2):c.408G>A (p.Met136Ile) rs1555977799
NM_005765.3(ATP6AP2):c.463C>T (p.Arg155Cys) rs146371390
NM_005765.3(ATP6AP2):c.490G>A (p.Val164Ile) rs142013283
NM_005765.3(ATP6AP2):c.50A>G (p.Asn17Ser)
NM_005765.3(ATP6AP2):c.596G>A (p.Arg199His) rs751433380
NM_005765.3(ATP6AP2):c.840C>G (p.Ile280Met) rs1555978066
NM_005765.3(ATP6AP2):c.858G>A (p.Ala286=) rs1555978069
NM_005765.3(ATP6AP2):c.922A>C (p.Asn308His) rs756836341
NM_005765.3(ATP6AP2):c.953C>A (p.Ala318Asp) rs1555978614

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