ClinVar Miner

List of variants in gene KIF11 reported as likely pathogenic for lymphoid system disorder

Included ClinVar conditions (123):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 38
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HGVS dbSNP gnomAD frequency
NG_032580.1:g.(92613040_92613130)_(92613377_92613619)del
NM_004523.4(KIF11):c.1060dup (p.His354fs)
NM_004523.4(KIF11):c.1235T>G (p.Leu412Ter)
NM_004523.4(KIF11):c.1305+1G>A rs1589600695
NM_004523.4(KIF11):c.1345C>T (p.Gln449Ter)
NM_004523.4(KIF11):c.139C>T (p.Arg47Ter)
NM_004523.4(KIF11):c.143_147del (p.Lys48fs)
NM_004523.4(KIF11):c.1513_1516del (p.Glu505fs)
NM_004523.4(KIF11):c.1580A>T (p.Asn527Ile) rs1844750166
NM_004523.4(KIF11):c.1634T>C (p.Met545Thr) rs1564713037
NM_004523.4(KIF11):c.1703-1G>A
NM_004523.4(KIF11):c.1935_1936del (p.Ser646fs)
NM_004523.4(KIF11):c.1A>G (p.Met1Val)
NM_004523.4(KIF11):c.2059del (p.His687fs) rs1554862197
NM_004523.4(KIF11):c.2268-1G>A
NM_004523.4(KIF11):c.2312_2313del (p.Lys771fs) rs1844907904
NM_004523.4(KIF11):c.2458G>T (p.Glu820Ter)
NM_004523.4(KIF11):c.2514_2518del (p.Asn838fs)
NM_004523.4(KIF11):c.2545G>T (p.Glu849Ter)
NM_004523.4(KIF11):c.2598_2601del (p.Gly868fs)
NM_004523.4(KIF11):c.2921dup (p.Asp975fs)
NM_004523.4(KIF11):c.2972dup (p.Ser992fs) rs1554863246
NM_004523.4(KIF11):c.301_302del (p.Ile101fs)
NM_004523.4(KIF11):c.376dup (p.Thr126fs) rs2135901156
NM_004523.4(KIF11):c.381G>A (p.Trp127Ter) rs1589590737
NM_004523.4(KIF11):c.422A>T (p.His141Leu) rs1844462612
NM_004523.4(KIF11):c.473del (p.Val158fs) rs2135902435
NM_004523.4(KIF11):c.489del (p.Tyr164fs)
NM_004523.4(KIF11):c.529del (p.Asp177fs)
NM_004523.4(KIF11):c.574-2A>G
NM_004523.4(KIF11):c.587_590del (p.Ile196fs)
NM_004523.4(KIF11):c.699-1G>C rs2135904871
NM_004523.4(KIF11):c.789+1G>T rs2135904919
NM_004523.4(KIF11):c.862_871del (p.Ile288fs) rs1057518980
NM_004523.4(KIF11):c.895A>G (p.Ile299Val) rs1844517913
NM_004523.4(KIF11):c.89T>A (p.Leu30Ter)
NM_004523.4(KIF11):c.934C>T (p.Arg312Ter) rs2135905068
NM_004523.4(KIF11):c.961C>T (p.Gln321Ter)

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