List of variants in gene KIF11 reported by Genetic Services Laboratory, University of Chicago

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 28

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HGVS	dbSNP	gnomAD frequency
NM_004523.4(KIF11):c.2771-6T>A	rs75876570	0.00444
NM_004523.4(KIF11):c.2166T>G (p.Leu722=)	rs147721514	0.00204
NM_004523.4(KIF11):c.1879G>T (p.Val627Leu)	rs142601912	0.00128
NM_004523.4(KIF11):c.2044C>G (p.Leu682Val)	rs141856144	0.00126
NM_004523.4(KIF11):c.2512A>C (p.Asn838His)	rs34647366	0.00074
NM_004523.4(KIF11):c.2775G>A (p.Thr925=)	rs138462002	0.00047
NM_004523.4(KIF11):c.77+5G>C	rs200188195	0.00031
NM_004523.4(KIF11):c.193A>G (p.Thr65Ala)	rs200410468	0.00009
NM_004523.4(KIF11):c.455C>T (p.Thr152Ile)	rs140534766	0.00004
NM_004523.4(KIF11):c.2106G>T (p.Lys702Asn)	rs189734472	0.00003
NM_004523.4(KIF11):c.1075A>G (p.Ile359Val)	rs1457816296	0.00001
NM_004523.4(KIF11):c.1677G>A (p.Met559Ile)	rs750869480	0.00001
NM_004523.4(KIF11):c.2562T>C (p.Cys854=)	rs963806889	0.00001
NM_004523.4(KIF11):c.690A>G (p.Ala230=)	rs759542620	0.00001
NM_004523.4(KIF11):c.-1_2delinsAA (p.Met1fs)	rs797045649
NM_004523.4(KIF11):c.112del (p.His38fs)	rs1554859309
NM_004523.4(KIF11):c.1305G>A (p.Arg435=)	rs1554861552
NM_004523.4(KIF11):c.179A>T (p.Lys60Met)	rs1298166671
NM_004523.4(KIF11):c.2018dup (p.Glu674fs)	rs1589604288
NM_004523.4(KIF11):c.2059del (p.His687fs)	rs1554862197
NM_004523.4(KIF11):c.2105del (p.Lys702fs)	rs2135919274
NM_004523.4(KIF11):c.2160+1G>T	rs1554862218
NM_004523.4(KIF11):c.2461T>C (p.Ser821Pro)	rs2135923469
NM_004523.4(KIF11):c.2548-1G>A	rs1554863016
NM_004523.4(KIF11):c.2922G>A (p.Pro974=)
NM_004523.4(KIF11):c.436A>T (p.Lys146Ter)	rs797045650
NM_004523.4(KIF11):c.699-7_705del	rs797045651
NM_004523.4(KIF11):c.868C>T (p.Gln290Ter)	rs1554859966

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