Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
7 | g.107690132T>A | CA457090207 | SLC26A4 | c.1158T>A (p.Ile386=) | |
7 | g.107690132T>C | CA457090205 | SLC26A4 | c.1158T>C (p.Ile386=) | |
7 | g.107690132T>G | CA368839122 | SLC26A4 | c.1158T>G (p.Ile386Met) | |
7 | g.107690133G>A | CA368839123 | SLC26A4 | c.1159G>A (p.Ala387Thr) | |
7 | g.107690133G>C | CA368839127 | SLC26A4 | c.1159G>C (p.Ala387Pro) | |
7 | g.107690133G>T | CA368839129 | SLC26A4 | c.1159G>T (p.Ala387Ser) | ClinVar |
7 | g.107690134C>A | CA4432712 | SLC26A4 | c.1160C>A (p.Ala387Asp) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
7 | g.107690134C= | CA1732748209 | SLC26A4 | c.1160C= (p.Ala387=) | |
7 | g.107690134C>G | CA368839130 | SLC26A4 | c.1160C>G (p.Ala387Gly) | |
7 | g.107690134C>T | CA4432713 | SLC26A4 | c.1160C>T (p.Ala387Val) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
7 | g.107690135C>A | CA457090231 | SLC26A4 | c.1161C>A (p.Ala387=) | gnomAD v4 |
7 | g.107690135C= | CA1732748214 | SLC26A4 | c.1161C= (p.Ala387=) | |
7 | g.107690135C>G | CA457090229 | SLC26A4 | c.1161C>G (p.Ala387=) | |
7 | g.107690135C>T | CA457090221 | SLC26A4 | c.1161C>T (p.Ala387=) | |
7 | g.107690136T>A | CA368839131 | SLC26A4 | c.1162T>A (p.Phe388Ile) | |
7 | g.107690136T>C | CA368839132 | SLC26A4 | c.1162T>C (p.Phe388Leu) | |
7 | g.107690136T>G | CA368839133 | SLC26A4 | c.1162T>G (p.Phe388Val) | |
7 | g.107690138dup | CA645372448 | SLC26A4 | c.1164dup (p.Gly389TrpfsTer?) | ClinVar dbSNP |
7 | g.107690137T>A | CA368839136 | SLC26A4 | c.1163T>A (p.Phe388Tyr) | |
7 | g.107690137T>C | CA368839135 | SLC26A4 | c.1163T>C (p.Phe388Ser) | |
7 | g.107690137T>G | CA368839134 | SLC26A4 | c.1163T>G (p.Phe388Cys) | |
7 | g.107690138T>A | CA368839137 | SLC26A4 | c.1164T>A (p.Phe388Leu) | |
7 | g.107690138T>C | CA457090257 | SLC26A4 | c.1164T>C (p.Phe388=) | |
7 | g.107690138T>G | CA368839138 | SLC26A4 | c.1164T>G (p.Phe388Leu) | |
7 | g.107690139G>A | CA368839139 | SLC26A4 | c.1165G>A (p.Gly389Arg) | dbSNP gnomAD v4 COSMIC |
7 | g.107690139G>C | CA368839140 | SLC26A4 | c.1165G>C (p.Gly389Arg) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
7 | g.107690139G= | CA1732748223 | SLC26A4 | c.1165G= (p.Gly389=) | |
7 | g.107690139G>T | CA368839141 | SLC26A4 | c.1165G>T (p.Gly389Trp) | dbSNP gnomAD v4 |
7 | g.107690140G>A | CA368839142 | SLC26A4 | c.1166G>A (p.Gly389Glu) | |
7 | g.107690140G>C | CA368839143 | SLC26A4 | c.1166G>C (p.Gly389Ala) | |
7 | g.107690140G>T | CA368839144 | SLC26A4 | c.1166G>T (p.Gly389Val) | |
7 | g.107690141G>A | CA457090281 | SLC26A4 | c.1167G>A (p.Gly389=) | dbSNP |
7 | g.107690141G>C | CA457090283 | SLC26A4 | c.1167G>C (p.Gly389=) | gnomAD v4 |
7 | g.107690141G= | CA1732748227 | SLC26A4 | c.1167G= (p.Gly389=) | |
7 | g.107690141G>T | CA457090288 | SLC26A4 | c.1167G>T (p.Gly389=) | |
7 | g.107690142A>C | CA368839145 | SLC26A4 | c.1168A>C (p.Ile390Leu) | |
7 | g.107690142A>G | CA368839146 | SLC26A4 | c.1168A>G (p.Ile390Val) | |
7 | g.107690142A>T | CA368839147 | SLC26A4 | c.1168A>T (p.Ile390Phe) | |
7 | g.107690143T>A | CA368839148 | SLC26A4 | c.1169T>A (p.Ile390Asn) | dbSNP |
7 | g.107690143T>C | CA368839149 | SLC26A4 | c.1169T>C (p.Ile390Thr) | |
7 | g.107690143T>G | CA368839150 | SLC26A4 | c.1169T>G (p.Ile390Ser) | |
7 | g.107690143T= | CA1732748230 | SLC26A4 | c.1169T= (p.Ile390=) | |
7 | g.107690144C>A | CA457090313 | SLC26A4 | c.1170C>A (p.Ile390=) | |
7 | g.107690144C= | CA1732748233 | SLC26A4 | c.1170C= (p.Ile390=) | |
7 | g.107690144C>G | CA368839151 | SLC26A4 | c.1170C>G (p.Ile390Met) | dbSNP gnomAD v2 gnomAD v4 |
7 | g.107690144C>T | CA457090318 | SLC26A4 | c.1170C>T (p.Ile390=) | COSMIC |
7 | g.107690145A= | CA1732748238 | SLC26A4 | c.1171A= (p.Ser391=) | |
7 | g.107690145A>C | CA368839153 | SLC26A4 | c.1171A>C (p.Ser391Arg) | ClinVar dbSNP |
7 | g.107690145A>G | CA368839152 | SLC26A4 | c.1171A>G (p.Ser391Gly) | gnomAD v4 |
7 | g.107690145A>T | CA368839154 | SLC26A4 | c.1171A>T (p.Ser391Cys) |