ClinVar Miner

List of variants in gene KIF1B reported as likely benign for not provided

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 43
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_001365951.3(KIF1B):c.608+8dup rs139613776 0.01962
NM_001365951.3(KIF1B):c.2115+6360G>T rs41274458 0.01961
NM_001365951.3(KIF1B):c.5432C>T (p.Pro1811Leu) rs61999305 0.01293
NM_001365951.3(KIF1B):c.4798G>A (p.Val1600Met) rs77172218 0.01096
NM_001365951.3(KIF1B):c.2115+6956A>G rs148481786 0.00525
NM_001365951.3(KIF1B):c.4158G>A (p.Ser1386=) rs116302604 0.00481
NM_001365951.3(KIF1B):c.5250A>G (p.Ala1750=) rs75413741 0.00415
NM_001365951.3(KIF1B):c.2115+6183T>C rs149241091 0.00357
NM_001365951.3(KIF1B):c.2115+7031T>C rs149267056 0.00320
NM_001365951.3(KIF1B):c.3635C>T (p.Pro1212Leu) rs141224290 0.00255
NM_001365951.3(KIF1B):c.2330A>G (p.Asn777Ser) rs117525287 0.00228
NM_001365951.3(KIF1B):c.4596C>T (p.Pro1532=) rs147066476 0.00150
NM_001365951.3(KIF1B):c.2115+6625G>A rs145248590 0.00129
NM_001365951.3(KIF1B):c.3259+9A>G rs149566646 0.00118
NM_001365951.3(KIF1B):c.3645G>A (p.Pro1215=) rs147318592 0.00092
NM_001365951.3(KIF1B):c.2115+6581G>A rs41274460 0.00089
NM_001365951.3(KIF1B):c.2115+5958G>A rs150181429 0.00050
NM_001365951.3(KIF1B):c.2618C>T (p.Thr873Ile) rs121908162 0.00040
NM_001365951.3(KIF1B):c.2604C>T (p.Asp868=) rs145846362 0.00031
NM_001365951.3(KIF1B):c.2115+6835C>T rs140733878 0.00026
NM_001365951.3(KIF1B):c.3636G>A (p.Pro1212=) rs140229905 0.00019
NM_001365951.3(KIF1B):c.2985C>T (p.Ile995=) rs150904940 0.00018
NM_001365951.3(KIF1B):c.4338A>G (p.Leu1446=) rs143112560 0.00014
NM_001365951.3(KIF1B):c.899A>G (p.Lys300Arg) rs373698346 0.00009
NM_001365951.3(KIF1B):c.107-8T>A rs749389756 0.00006
NM_001365951.3(KIF1B):c.1122G>A (p.Glu374=) rs774770887 0.00003
NM_001365951.3(KIF1B):c.2586G>A (p.Met862Ile) rs199818954 0.00003
NM_001365951.3(KIF1B):c.1782C>T (p.Ile594=) rs774839409 0.00002
NM_001365951.3(KIF1B):c.3756C>A (p.Leu1252=) rs1341773631 0.00002
NM_001365951.3(KIF1B):c.1680A>G (p.Gln560=) rs765720258 0.00001
NM_001365951.3(KIF1B):c.3849A>G (p.Thr1283=) rs746980680 0.00001
NM_001365951.3(KIF1B):c.1162C>T (p.Leu388=) rs1569678310
NM_001365951.3(KIF1B):c.1263A>G (p.Leu421=)
NM_001365951.3(KIF1B):c.2115+5919C>T
NM_001365951.3(KIF1B):c.2115+6312C>T
NM_001365951.3(KIF1B):c.2115+6891G>A
NM_001365951.3(KIF1B):c.2115+7116G>A rs1334941848
NM_001365951.3(KIF1B):c.2115+7274A>G
NM_001365951.3(KIF1B):c.3216G>A (p.Glu1072=)
NM_001365951.3(KIF1B):c.3393A>C (p.Pro1131=) rs1569854004
NM_001365951.3(KIF1B):c.3909G>C (p.Gly1303=) rs1569872691
NM_001365951.3(KIF1B):c.4365A>G (p.Pro1455=)
NM_001365951.3(KIF1B):c.525A>T (p.Gly175=)

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.