Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
15 | g.73343622T>A | CA491479801 | HCN4 | c.972A>T (p.Thr324=) | |
15 | g.73343622T>C | CA7649391 | HCN4 | c.972A>G (p.Thr324=) | ClinVar dbSNP ExAC gnomAD v3 gnomAD v4 |
15 | g.73343622T>G | CA491479802 | HCN4 | c.972A>C (p.Thr324=) | |
15 | g.73343622T= | CA2187180019 | HCN4 | c.972A= (p.Thr324=) | |
15 | g.73343623G>A | CA393095135 | HCN4 | c.971C>T (p.Thr324Ile) | |
15 | g.73343623G>C | CA393095136 | HCN4 | c.971C>G (p.Thr324Arg) | |
15 | g.73343623G>T | CA393095134 | HCN4 | c.971C>A (p.Thr324Lys) | |
15 | g.73343624T>A | CA393095137 | HCN4 | c.970A>T (p.Thr324Ser) | |
15 | g.73343624T>C | CA393095138 | HCN4 | c.970A>G (p.Thr324Ala) | dbSNP gnomAD v3 gnomAD v4 |
15 | g.73343624T>G | CA393095139 | HCN4 | c.970A>C (p.Thr324Pro) | |
15 | g.73343624T= | CA2187180026 | HCN4 | c.970A= (p.Thr324=) | |
15 | g.73343625G>A | CA491479803 | HCN4 | c.969C>T (p.Asn323=) | |
15 | g.73343625G>C | CA393095140 | HCN4 | c.969C>G (p.Asn323Lys) | |
15 | g.73343625G>T | CA393095141 | HCN4 | c.969C>A (p.Asn323Lys) | |
15 | g.73343626T>A | CA393095144 | HCN4 | c.968A>T (p.Asn323Ile) | |
15 | g.73343626T>C | CA393095142 | HCN4 | c.968A>G (p.Asn323Ser) | |
15 | g.73343626T>G | CA393095143 | HCN4 | c.968A>C (p.Asn323Thr) | |
15 | g.73343627T>A | CA393095145 | HCN4 | c.967A>T (p.Asn323Tyr) | |
15 | g.73343627T>C | CA393095146 | HCN4 | c.967A>G (p.Asn323Asp) | |
15 | g.73343627T>G | CA393095147 | HCN4 | c.967A>C (p.Asn323His) | |
15 | g.73343628G>A | CA7649392 | HCN4 | c.966C>T (p.Asp322=) | dbSNP ExAC gnomAD v2 gnomAD v4 |
15 | g.73343628G>C | CA393095148 | HCN4 | c.966C>G (p.Asp322Glu) | |
15 | g.73343628G= | CA2187180033 | HCN4 | c.966C= (p.Asp322=) | |
15 | g.73343628G>T | CA393095149 | HCN4 | c.966C>A (p.Asp322Glu) | |
15 | g.73343629T>A | CA393095151 | HCN4 | c.965A>T (p.Asp322Val) | |
15 | g.73343629T>C | CA393095152 | HCN4 | c.965A>G (p.Asp322Gly) | |
15 | g.73343629T>G | CA393095150 | HCN4 | c.965A>C (p.Asp322Ala) | |
15 | g.73343630C>A | CA393095154 | HCN4 | c.964G>T (p.Asp322Tyr) | |
15 | g.73343630C>G | CA393095153 | HCN4 | c.964G>C (p.Asp322His) | |
15 | g.73343630C>T | CA393095155 | HCN4 | c.964G>A (p.Asp322Asn) | |
15 | g.73343631C>A | CA393095156 | HCN4 | c.963G>T (p.Glu321Asp) | |
15 | g.73343631C>G | CA393095157 | HCN4 | c.963G>C (p.Glu321Asp) | |
15 | g.73343631C>T | CA491479804 | HCN4 | c.963G>A (p.Glu321=) | |
15 | g.73343632T>A | CA393095158 | HCN4 | c.962A>T (p.Glu321Val) | COSMIC |
15 | g.73343632T>C | CA393095159 | HCN4 | c.962A>G (p.Glu321Gly) | |
15 | g.73343632T>G | CA393095160 | HCN4 | c.962A>C (p.Glu321Ala) | |
15 | g.73343633C>A | CA393095161 | HCN4 | c.961G>T (p.Glu321Ter) | |
15 | g.73343633C>G | CA393095162 | HCN4 | c.961G>C (p.Glu321Gln) | |
15 | g.73343633C>T | CA393095163 | HCN4 | c.961G>A (p.Glu321Lys) | |
15 | g.73343634C>A | CA491479807 | HCN4 | c.960G>T (p.Val320=) | |
15 | g.73343634C= | CA2187180038 | HCN4 | c.960G= (p.Val320=) | |
15 | g.73343634C>G | CA491479806 | HCN4 | c.960G>C (p.Val320=) | |
15 | g.73343634C>T | CA491479805 | HCN4 | c.960G>A (p.Val320=) | dbSNP gnomAD v2 gnomAD v4 COSMIC |
15 | g.73343635A>C | CA393095164 | HCN4 | c.959T>G (p.Val320Gly) | |
15 | g.73343635A>G | CA393095165 | HCN4 | c.959T>C (p.Val320Ala) | gnomAD v4 |
15 | g.73343635A>T | CA393095166 | HCN4 | c.959T>A (p.Val320Glu) | |
15 | g.73343636C>A | CA393095167 | HCN4 | c.958G>T (p.Val320Leu) | |
15 | g.73343636C>G | CA393095168 | HCN4 | c.958G>C (p.Val320Leu) | |
15 | g.73343636C>T | CA393095169 | HCN4 | c.958G>A (p.Val320Met) | COSMIC |
15 | g.73343637C>A | CA491479808 | HCN4 | c.957G>T (p.Val319=) |