ClinVar Miner

List of variants in gene WIPF1 reported as likely benign 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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HGVS dbSNP
NM_001077269.1(WIPF1):c.1037C>T (p.Pro346Leu) rs149434153
NM_001077269.1(WIPF1):c.1116G>A (p.Pro372=) rs138920689
NM_001077269.1(WIPF1):c.1170C>T (p.Ser390=) rs1205840828
NM_001077269.1(WIPF1):c.1380C>T (p.Ser460=) rs753915750
NM_001077269.1(WIPF1):c.1497T>A (p.Pro499=) rs749710168
NM_001077269.1(WIPF1):c.212G>A (p.Gly71Asp) rs145037448
NM_001077269.1(WIPF1):c.243C>T (p.Gly81=) rs146533814
NM_001077269.1(WIPF1):c.30G>A (p.Pro10=) rs745425874
NM_001077269.1(WIPF1):c.32C>T (p.Pro11Leu) rs148943760
NM_001077269.1(WIPF1):c.936T>G (p.Pro312=) rs1040586347
NM_001077269.1(WIPF1):c.975C>G (p.Ser325=) rs751419161
NM_001077269.1(WIPF1):c.978C>G (p.Ser326Arg) rs147080148
NM_001077269.1(WIPF1):c.987C>T (p.Asp329=) rs201234000
NM_003387.5(WIPF1):c.851_853CTC[5] (p.Pro287dup) rs556678311

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