ClinVar Miner

List of variants in gene KIF11 reported as uncertain significance for immune system disorder

Included ClinVar conditions (908):
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Gene type:
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Total variants: 24
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HGVS dbSNP gnomAD frequency
NM_004523.4(KIF11):c.193A>G (p.Thr65Ala) rs200410468 0.00009
NM_004523.4(KIF11):c.980G>A (p.Arg327His) rs746977730 0.00006
NM_004523.4(KIF11):c.1677G>A (p.Met559Ile) rs750869480 0.00001
NM_004523.4(KIF11):c.1823T>C (p.Leu608Pro) rs535517017 0.00001
NM_004523.4(KIF11):c.2089T>G (p.Leu697Val) rs781259791 0.00001
NM_004523.4(KIF11):c.1217+14_1217+283del rs1844616530
NM_004523.4(KIF11):c.131A>G (p.Asp44Gly) rs1844430488
NM_004523.4(KIF11):c.1480G>A (p.Asp494Asn)
NM_004523.4(KIF11):c.151A>G (p.Ser51Gly) rs1844430675
NM_004523.4(KIF11):c.1559A>G (p.Lys520Arg) rs2135916166
NM_004523.4(KIF11):c.1875+4A>G
NM_004523.4(KIF11):c.1879G>A (p.Val627Ile)
NM_004523.4(KIF11):c.209T>C (p.Met70Thr)
NM_004523.4(KIF11):c.2160+5G>A
NM_004523.4(KIF11):c.2279A>T (p.Asp760Val) rs778431479
NM_004523.4(KIF11):c.2369G>C (p.Gly790Ala)
NM_004523.4(KIF11):c.2654C>A (p.Thr885Asn)
NM_004523.4(KIF11):c.2704A>G (p.Ile902Val)
NM_004523.4(KIF11):c.2804C>T (p.Pro935Leu)
NM_004523.4(KIF11):c.349G>T (p.Gly117Cys) rs1589590723
NM_004523.4(KIF11):c.388-6T>G
NM_004523.4(KIF11):c.532G>C (p.Val178Leu)
NM_004523.4(KIF11):c.704C>G (p.Ser235Cys) rs387906643
NM_004523.4(KIF11):c.733A>G (p.Met245Val) rs1403095180

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