ClinVar Miner

List of variants in gene ANKRD1 reported as likely benign for Cardiovascular phenotype

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 38
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_014391.3(ANKRD1):c.319G>T (p.Val107Leu) rs114435632 0.00269
NM_014391.3(ANKRD1):c.197G>A (p.Arg66Gln) rs150797476 0.00092
NM_014391.3(ANKRD1):c.369G>A (p.Thr123=) rs148979787 0.00069
NM_014391.3(ANKRD1):c.818T>C (p.Met273Thr) rs183061595 0.00039
NM_014391.3(ANKRD1):c.449A>T (p.Asp150Val) rs150266349 0.00019
NM_014391.3(ANKRD1):c.441T>C (p.Asp147=) rs145827106 0.00018
NM_014391.3(ANKRD1):c.603T>G (p.Val201=) rs781049118 0.00015
NM_014391.3(ANKRD1):c.108T>C (p.Ala36=) rs145211719 0.00009
NM_014391.3(ANKRD1):c.150C>G (p.Ala50=) rs147484763 0.00006
NM_014391.3(ANKRD1):c.496T>C (p.Leu166=) rs550582183 0.00004
NM_014391.3(ANKRD1):c.545G>A (p.Arg182His) rs530739375 0.00004
NM_014391.3(ANKRD1):c.669G>A (p.Leu223=) rs1425477748 0.00004
NM_014391.3(ANKRD1):c.531C>A (p.Ala177=) rs752596944 0.00002
NM_014391.3(ANKRD1):c.165G>C (p.Leu55=) rs375414155 0.00001
NM_014391.3(ANKRD1):c.256G>C (p.Asp86His) rs573892607 0.00001
NM_014391.3(ANKRD1):c.318T>C (p.Val106=) rs768982146 0.00001
NM_014391.3(ANKRD1):c.450T>C (p.Asp150=) rs775789003 0.00001
NM_014391.3(ANKRD1):c.560C>T (p.Ser187Phe) rs397517251 0.00001
NM_014391.3(ANKRD1):c.678G>A (p.Ala226=) rs376432423 0.00001
NM_014391.3(ANKRD1):c.135G>C (p.Leu45=) rs1589510792
NM_014391.3(ANKRD1):c.186C>T (p.Ser62=)
NM_014391.3(ANKRD1):c.21G>A (p.Glu7=)
NM_014391.3(ANKRD1):c.286A>C (p.Arg96=)
NM_014391.3(ANKRD1):c.299G>A (p.Arg100Lys)
NM_014391.3(ANKRD1):c.330A>C (p.Pro110=)
NM_014391.3(ANKRD1):c.346-29_346-12del rs72003210
NM_014391.3(ANKRD1):c.471T>G (p.Leu157=)
NM_014391.3(ANKRD1):c.549T>C (p.Asp183=)
NM_014391.3(ANKRD1):c.54G>A (p.Gly18=) rs763573338
NM_014391.3(ANKRD1):c.72T>C (p.Leu24=)
NM_014391.3(ANKRD1):c.732C>T (p.Asp244=)
NM_014391.3(ANKRD1):c.751-4C>G
NM_014391.3(ANKRD1):c.75T>C (p.Pro25=)
NM_014391.3(ANKRD1):c.810C>T (p.Leu270=)
NM_014391.3(ANKRD1):c.876G>A (p.Val292=)
NM_014391.3(ANKRD1):c.897C>T (p.Thr299=) rs1028634898
NM_014391.3(ANKRD1):c.924G>A (p.Glu308=)
NM_014391.3(ANKRD1):c.927C>T (p.Asn309=)

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.