ClinVar Miner

List of variants in gene SLC26A4 reported as uncertain significance for not provided

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 33
Download table as spreadsheet
HGVS dbSNP
NM_000441.1(SLC26A4):c.28C>A (p.Pro10Thr) rs200102493
NM_000441.2(SLC26A4):c.-103T>C rs60284988
NM_000441.2(SLC26A4):c.1014T>G (p.Pro338=)
NM_000441.2(SLC26A4):c.1040C>T (p.Ser347Leu) rs150946659
NM_000441.2(SLC26A4):c.1061T>C (p.Phe354Ser) rs111033243
NM_000441.2(SLC26A4):c.1233C>T (p.Ala411=) rs766572560
NM_000441.2(SLC26A4):c.1301C>A (p.Ala434Asp) rs1035397261
NM_000441.2(SLC26A4):c.1383G>T (p.Met461Ile) rs1367992231
NM_000441.2(SLC26A4):c.1412T>C (p.Leu471Pro) rs1562835716
NM_000441.2(SLC26A4):c.147C>G (p.Ser49Arg) rs756969021
NM_000441.2(SLC26A4):c.1572C>T (p.Ile524=) rs1562837305
NM_000441.2(SLC26A4):c.1614C>T (p.Asn538=) rs111033193
NM_000441.2(SLC26A4):c.1616T>C (p.Ile539Thr) rs146269871
NM_000441.2(SLC26A4):c.1673A>G (p.Asn558Ser) rs766206507
NM_000441.2(SLC26A4):c.1701G>C (p.Lys567Asn)
NM_000441.2(SLC26A4):c.1708-1G>A rs759414956
NM_000441.2(SLC26A4):c.1730T>C (p.Val577Ala) rs56017519
NM_000441.2(SLC26A4):c.1766A>C (p.Gln589Pro) rs397516422
NM_000441.2(SLC26A4):c.1852G>A (p.Asp618Asn) rs886043208
NM_000441.2(SLC26A4):c.1905G>A (p.Glu635=) rs541538556
NM_000441.2(SLC26A4):c.1957G>C (p.Val653Leu) rs1554361014
NM_000441.2(SLC26A4):c.2047T>G (p.Phe683Val) rs959216005
NM_000441.2(SLC26A4):c.2219G>T (p.Gly740Val) rs111033310
NM_000441.2(SLC26A4):c.2227T>G (p.Leu743Val) rs780626619
NM_000441.2(SLC26A4):c.227C>G (p.Pro76Arg)
NM_000441.2(SLC26A4):c.2283A>G (p.Thr761=) rs202033028
NM_000441.2(SLC26A4):c.236G>A (p.Arg79Gln) rs200706874
NM_000441.2(SLC26A4):c.247T>G (p.Trp83Gly) rs1584294942
NM_000441.2(SLC26A4):c.441G>A (p.Met147Ile) rs201905280
NM_000441.2(SLC26A4):c.475G>A (p.Glu159Lys) rs1562823659
NM_000441.2(SLC26A4):c.535G>A (p.Ala179Thr) rs114473792
NM_000441.2(SLC26A4):c.845G>A (p.Cys282Tyr) rs111033454
NM_000441.2(SLC26A4):c.859G>C (p.Glu287Gln) rs1584317605

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.