ClinVar Miner

List of variants in gene ANXA11 reported as uncertain significance for Inborn genetic diseases

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 43
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_145868.2(ANXA11):c.1457C>T (p.Ser486Leu) rs778082972 0.00020
NM_145868.2(ANXA11):c.399G>T (p.Met133Ile) rs111372395 0.00020
NM_145868.2(ANXA11):c.670A>G (p.Ile224Val) rs146991024 0.00014
NM_145868.2(ANXA11):c.1061T>C (p.Met354Thr) rs373296075 0.00013
NM_145868.2(ANXA11):c.89C>G (p.Pro30Arg) rs758548370 0.00009
NM_145868.2(ANXA11):c.595G>A (p.Gly199Ser) rs200982603 0.00008
NM_145868.2(ANXA11):c.173C>T (p.Ala58Val) rs761377370 0.00007
NM_145868.2(ANXA11):c.183G>A (p.Met61Ile) rs2492160106 0.00005
NM_145868.2(ANXA11):c.113G>A (p.Gly38Glu) rs1002251764 0.00004
NM_145868.2(ANXA11):c.1328C>A (p.Ala443Asp) rs1000931056 0.00003
NM_145868.2(ANXA11):c.944A>G (p.Lys315Arg) rs372493671 0.00002
NM_145868.2(ANXA11):c.100A>G (p.Met34Val) rs762135310 0.00001
NM_145868.2(ANXA11):c.1081G>A (p.Ala361Thr) rs767049795 0.00001
NM_145868.2(ANXA11):c.130A>G (p.Thr44Ala) rs539258237 0.00001
NM_145868.2(ANXA11):c.164C>T (p.Ser55Leu) rs1416413633 0.00001
NM_145868.2(ANXA11):c.190A>G (p.Thr64Ala) rs775879177 0.00001
NM_145868.2(ANXA11):c.403C>T (p.Pro135Ser) rs747262502 0.00001
NM_145868.2(ANXA11):c.517T>C (p.Tyr173His) rs748980504 0.00001
NM_145868.2(ANXA11):c.644G>C (p.Gly215Ala) rs758009574 0.00001
NM_145868.2(ANXA11):c.739G>A (p.Gly247Ser) rs147883184 0.00001
NM_145868.2(ANXA11):c.74G>A (p.Gly25Asp) rs770526320 0.00001
NM_145868.2(ANXA11):c.100A>C (p.Met34Leu) rs762135310
NM_145868.2(ANXA11):c.1062G>A (p.Met354Ile)
NM_145868.2(ANXA11):c.1102G>A (p.Gly368Arg) rs772333853
NM_145868.2(ANXA11):c.1102G>C (p.Gly368Arg)
NM_145868.2(ANXA11):c.1126G>A (p.Glu376Lys)
NM_145868.2(ANXA11):c.1130C>G (p.Ser377Cys)
NM_145868.2(ANXA11):c.1363A>T (p.Ile455Phe)
NM_145868.2(ANXA11):c.1409G>C (p.Arg470Thr)
NM_145868.2(ANXA11):c.158A>G (p.Tyr53Cys) rs766285457
NM_145868.2(ANXA11):c.368A>G (p.Tyr123Cys) rs760158626
NM_145868.2(ANXA11):c.376G>T (p.Ala126Ser)
NM_145868.2(ANXA11):c.437G>A (p.Gly146Glu) rs2492155132
NM_145868.2(ANXA11):c.533C>G (p.Thr178Ser)
NM_145868.2(ANXA11):c.542C>T (p.Pro181Leu)
NM_145868.2(ANXA11):c.656A>G (p.Asp219Gly)
NM_145868.2(ANXA11):c.674A>G (p.Asp225Gly) rs1305559152
NM_145868.2(ANXA11):c.676T>C (p.Cys226Arg)
NM_145868.2(ANXA11):c.67T>C (p.Trp23Arg) rs2492174002
NM_145868.2(ANXA11):c.688C>A (p.Arg230Ser) rs1049550
NM_145868.2(ANXA11):c.699G>C (p.Lys233Asn) rs2492132042
NM_145868.2(ANXA11):c.701A>G (p.Gln234Arg)
NM_145868.2(ANXA11):c.862G>A (p.Val288Ile) rs374621104

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.