ClinVar Miner

List of variants in gene KIF5A reported as likely benign by GeneDx

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 58
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_004984.4(KIF5A):c.1716+286G>A rs113973631 0.01951
NM_004984.4(KIF5A):c.502-258C>T rs141016935 0.01775
NM_004984.4(KIF5A):c.501+43A>C rs77884162 0.01293
NM_004984.4(KIF5A):c.3021-55T>C rs189141503 0.01060
NM_004984.4(KIF5A):c.1569+119G>A rs111481780 0.00883
NM_004984.4(KIF5A):c.1906-143T>A rs76164219 0.00882
NM_004984.4(KIF5A):c.1294-173T>C rs143272215 0.00771
NM_004984.4(KIF5A):c.1362+125T>C rs116317869 0.00767
NM_004984.4(KIF5A):c.714+200G>A rs149354963 0.00760
NM_004984.4(KIF5A):c.292-42C>T rs148481427 0.00713
NM_004984.4(KIF5A):c.502-59A>G rs117149568 0.00672
NM_004984.4(KIF5A):c.501+307G>A rs140470142 0.00584
NM_004984.4(KIF5A):c.*36+164G>T rs114224724 0.00558
NM_004984.4(KIF5A):c.1569+21C>G rs114115696 0.00558
NM_004984.4(KIF5A):c.2198+190A>T rs114284372 0.00556
NM_004984.4(KIF5A):c.292-173A>G rs114419475 0.00556
NM_004984.4(KIF5A):c.1905+126G>A rs114614349 0.00555
NM_004984.4(KIF5A):c.2198+189G>T rs115809275 0.00555
NM_004984.4(KIF5A):c.2993-302C>T rs115689942 0.00555
NM_004984.4(KIF5A):c.820-82C>T rs116892071 0.00477
NM_004984.4(KIF5A):c.2993-293G>C rs148806802 0.00445
NM_004984.4(KIF5A):c.2024-106T>C rs536469610 0.00326
NM_004984.4(KIF5A):c.1293+9G>A rs201749114 0.00222
NM_004984.4(KIF5A):c.714+8G>A rs199624091 0.00101
NM_004984.4(KIF5A):c.1419G>A (p.Leu473=) rs139091551 0.00070
NM_004984.4(KIF5A):c.1716+51C>T rs373997459 0.00064
NM_004984.4(KIF5A):c.1150G>C (p.Gly384Arg) rs143326964 0.00060
NM_004984.4(KIF5A):c.471C>T (p.His157=) rs143178113 0.00034
NM_004984.4(KIF5A):c.1363-22A>T rs373198221 0.00024
NM_004984.4(KIF5A):c.2718C>T (p.Tyr906=) rs147057295 0.00019
NM_004984.4(KIF5A):c.129+9C>T rs372131378 0.00016
NM_004984.4(KIF5A):c.2040G>A (p.Val680=) rs117670788 0.00016
NM_004984.4(KIF5A):c.2927C>T (p.Thr976Ile) rs139801016 0.00014
NM_004984.4(KIF5A):c.2775C>A (p.Gly925=) rs759750438 0.00009
NM_004984.4(KIF5A):c.2262C>T (p.Ser754=) rs143260492 0.00007
NM_004984.4(KIF5A):c.1118-41T>G rs376582946 0.00003
NM_004984.4(KIF5A):c.750C>T (p.Asp250=) rs375693647 0.00003
NM_004984.4(KIF5A):c.861T>C (p.Ile287=) rs1283311048 0.00003
NM_004984.4(KIF5A):c.1287C>T (p.Asp429=) rs760382029 0.00002
NM_004984.4(KIF5A):c.2655C>T (p.Gly885=) rs1007236664 0.00002
NM_004984.4(KIF5A):c.2990A>T (p.Asn997Ile) rs146202502 0.00002
NM_004984.4(KIF5A):c.-13G>A rs375902978 0.00001
NM_004984.4(KIF5A):c.1218G>C (p.Val406=) rs758977709 0.00001
NM_004984.4(KIF5A):c.1896C>T (p.Leu632=) rs1161979577 0.00001
NM_004984.4(KIF5A):c.2539-13G>A rs1057523621 0.00001
NM_004984.4(KIF5A):c.291+15T>C rs764730335 0.00001
NM_004984.4(KIF5A):c.2993-6C>T rs1057522322 0.00001
NM_004984.4(KIF5A):c.*36+95del rs35104895
NM_004984.4(KIF5A):c.2198+19G>T rs932182752
NM_004984.4(KIF5A):c.292-4C>A rs760970894
NM_004984.4(KIF5A):c.2992+100C>A rs111792924
NM_004984.4(KIF5A):c.2992+137dup rs1013090932
NM_004984.4(KIF5A):c.397-16_397-14del rs375316447
NM_004984.4(KIF5A):c.714+282dup rs538379606
NM_004984.4(KIF5A):c.714+58_714+60dup rs371727146
NM_004984.4(KIF5A):c.714+59_714+60dup rs371727146
NM_004984.4(KIF5A):c.715-225del rs558633353
NM_004984.4(KIF5A):c.715-323G>T rs142538303

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.