ClinVar Miner

List of variants in gene ACP6 studied for not specified

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 40
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_016361.5(ACP6):c.652C>T (p.Arg218Trp) rs140566115 0.01070
NM_016361.5(ACP6):c.112G>A (p.Asp38Asn) rs200702109 0.00023
NM_016361.5(ACP6):c.460T>A (p.Phe154Ile) rs146298808 0.00014
NM_016361.5(ACP6):c.301A>C (p.Lys101Gln) rs374575256 0.00013
NM_016361.5(ACP6):c.326A>G (p.Gln109Arg) rs140398965 0.00011
NM_016361.5(ACP6):c.134G>A (p.Arg45His) rs149388165 0.00004
NM_016361.5(ACP6):c.1113G>T (p.Glu371Asp) rs782395582 0.00003
NM_016361.5(ACP6):c.1206G>A (p.Met402Ile) rs782505855 0.00003
NM_016361.5(ACP6):c.712A>G (p.Arg238Gly) rs1443058005 0.00003
NM_016361.5(ACP6):c.769G>A (p.Ala257Thr) rs140258721 0.00002
NM_016361.5(ACP6):c.1138G>A (p.Gly380Arg) rs146616655 0.00001
NM_016361.5(ACP6):c.182C>G (p.Ala61Gly) rs1336514463 0.00001
NM_016361.5(ACP6):c.22A>G (p.Met8Val) rs1462870297 0.00001
NM_016361.5(ACP6):c.358T>A (p.Phe120Ile) rs1553212315 0.00001
NM_016361.5(ACP6):c.409G>A (p.Glu137Lys) rs781849731 0.00001
NM_016361.5(ACP6):c.502C>T (p.Arg168Trp) rs978886014 0.00001
NM_016361.5(ACP6):c.585A>C (p.Glu195Asp) rs146958747 0.00001
NM_016361.5(ACP6):c.766G>A (p.Val256Met) rs782552755 0.00001
NM_016361.5(ACP6):c.967G>A (p.Asp323Asn) rs782414489 0.00001
NM_016361.5(ACP6):c.1066G>A (p.Ala356Thr)
NM_016361.5(ACP6):c.1119T>A (p.Phe373Leu) rs782629079
NM_016361.5(ACP6):c.11G>A (p.Gly4Asp)
NM_016361.5(ACP6):c.1265T>C (p.Met422Thr) rs781853603
NM_016361.5(ACP6):c.19A>G (p.Ser7Gly)
NM_016361.5(ACP6):c.202C>G (p.Leu68Val)
NM_016361.5(ACP6):c.353G>A (p.Gly118Asp) rs1553212321
NM_016361.5(ACP6):c.419G>A (p.Arg140Lys)
NM_016361.5(ACP6):c.454C>T (p.Pro152Ser)
NM_016361.5(ACP6):c.485G>A (p.Arg162His)
NM_016361.5(ACP6):c.599T>G (p.Val200Gly) rs2526781694
NM_016361.5(ACP6):c.607C>T (p.Pro203Ser) rs2526781561
NM_016361.5(ACP6):c.629G>C (p.Ser210Thr)
NM_016361.5(ACP6):c.635G>A (p.Arg212Lys) rs2526781268
NM_016361.5(ACP6):c.660G>C (p.Gln220His) rs2526776925
NM_016361.5(ACP6):c.661A>G (p.Thr221Ala)
NM_016361.5(ACP6):c.673C>G (p.Gln225Glu) rs201893716
NM_016361.5(ACP6):c.733G>A (p.Asp245Asn) rs782246421
NM_016361.5(ACP6):c.784C>T (p.His262Tyr)
NM_016361.5(ACP6):c.815G>T (p.Arg272Ile)
NM_016361.5(ACP6):c.992A>T (p.Tyr331Phe)

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.