ClinVar Miner

List of variants in gene AKR1C3 reported by Ambry Genetics

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 35
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_003739.6(AKR1C3):c.826C>T (p.Arg276Cys) rs140613308 0.00067
NM_003739.6(AKR1C3):c.269A>G (p.His90Arg) rs200981816 0.00025
NM_003739.6(AKR1C3):c.818A>G (p.Asn273Ser) rs368182129 0.00010
NM_003739.6(AKR1C3):c.221T>C (p.Val74Ala) rs782157138 0.00004
NM_003739.6(AKR1C3):c.449C>T (p.Ala150Val) rs192314534 0.00003
NM_003739.6(AKR1C3):c.731T>G (p.Leu244Trp) rs1293610449 0.00003
NM_003739.6(AKR1C3):c.845A>C (p.Gln282Pro) rs1476551152 0.00003
NM_003739.6(AKR1C3):c.139C>T (p.Arg47Cys) rs150753542 0.00002
NM_003739.6(AKR1C3):c.425T>G (p.Val142Gly) rs782753500 0.00001
NM_003739.6(AKR1C3):c.812G>A (p.Ser271Asn) rs782266004 0.00001
NM_003739.6(AKR1C3):c.902G>C (p.Arg301Thr) rs782141648 0.00001
NM_003739.6(AKR1C3):c.101C>T (p.Ala34Val)
NM_003739.6(AKR1C3):c.121G>A (p.Ala41Thr)
NM_003739.6(AKR1C3):c.181G>C (p.Val61Leu)
NM_003739.6(AKR1C3):c.194T>G (p.Ile65Ser) rs782190855
NM_003739.6(AKR1C3):c.238T>C (p.Phe80Leu)
NM_003739.6(AKR1C3):c.321A>T (p.Gln107His) rs140441894
NM_003739.6(AKR1C3):c.323T>C (p.Leu108Ser)
NM_003739.6(AKR1C3):c.350A>G (p.His117Arg)
NM_003739.6(AKR1C3):c.386C>T (p.Ser129Leu)
NM_003739.6(AKR1C3):c.485C>T (p.Ser162Phe)
NM_003739.6(AKR1C3):c.501C>G (p.Asn167Lys) rs782171165
NM_003739.6(AKR1C3):c.512G>T (p.Arg171Met)
NM_003739.6(AKR1C3):c.556C>T (p.Pro186Ser)
NM_003739.6(AKR1C3):c.601A>G (p.Lys201Glu) rs536138448
NM_003739.6(AKR1C3):c.625A>G (p.Lys209Glu)
NM_003739.6(AKR1C3):c.632T>G (p.Ile211Ser) rs200858905
NM_003739.6(AKR1C3):c.681G>T (p.Trp227Cys) rs1554786231
NM_003739.6(AKR1C3):c.748C>G (p.Arg250Gly) rs782377695
NM_003739.6(AKR1C3):c.749G>A (p.Arg250Gln)
NM_003739.6(AKR1C3):c.758C>T (p.Ala253Val)
NM_003739.6(AKR1C3):c.829A>G (p.Ile277Val) rs1554786303
NM_003739.6(AKR1C3):c.847G>A (p.Val283Ile)
NM_003739.6(AKR1C3):c.928A>T (p.Ser310Cys) rs2491549207
NM_003739.6(AKR1C3):c.956A>C (p.Tyr319Ser)

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.