ClinVar Miner

List of variants in gene F11 reported as benign by Invitae

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 17
Download table as spreadsheet
HGVS dbSNP
NM_000128.3(F11):c.-54G>A rs4253814
NM_000128.3(F11):c.1016G>T (p.Cys339Phe) rs5967
NM_000128.3(F11):c.1191T>C (p.Gly397=) rs5970
NM_000128.3(F11):c.1305-9G>T rs4253426
NM_000128.3(F11):c.1707C>T (p.Asp569=) rs5975
NM_000128.3(F11):c.1812G>T (p.Arg604=) rs5971
NM_000128.3(F11):c.1839G>A (p.Glu613=) rs5976
NM_000128.3(F11):c.429C>T (p.Asp143=) rs5973
NM_000128.3(F11):c.731A>G (p.Gln244Arg) rs5969
NM_000128.3(F11):c.801A>G (p.Thr267=) rs5974
NM_000128.4(F11):c.1020C>T (p.Asn340=) rs149052026
NM_000128.4(F11):c.1304+12G>A
NM_000128.4(F11):c.1481-188C>T rs2289252
NM_000128.4(F11):c.1599G>A (p.Gln533=)
NM_000128.4(F11):c.453C>T (p.Tyr151=) rs34807019
NM_000128.4(F11):c.539A>G (p.Lys180Arg) rs190283743
NM_000128.4(F11):c.663C>T (p.Pro221=) rs142846329

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.