Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
11 | g.17387296G>A | CA379770658 | KCNJ11 | c.535C>T (p.Pro179Ser) c.796C>T (p.Pro266Ser) n.954C>T | COSMIC |
11 | g.17387296G>C | CA379770657 | KCNJ11 | c.535C>G (p.Pro179Ala) c.796C>G (p.Pro266Ala) n.954C>G | |
11 | g.17387296G= | CA1955119201 | KCNJ11 | c.535C= (p.Pro179=) c.796C= (p.Pro266=) n.954C= | |
11 | g.17387296G>T | CA379770656 | KCNJ11 | c.535C>A (p.Pro179Thr) c.796C>A (p.Pro266Thr) n.954C>A | |
11 | g.17387297G>A | CA473515413 | KCNJ11 | c.534C>T (p.Ser178=) c.795C>T (p.Ser265=) n.953C>T | ClinVar |
11 | g.17387297G>C | CA379770659 | KCNJ11 | c.534C>G (p.Ser178Arg) c.795C>G (p.Ser265Arg) n.953C>G | |
11 | g.17387297G>T | CA379770662 | KCNJ11 | c.534C>A (p.Ser178Arg) c.795C>A (p.Ser265Arg) n.953C>A | |
11 | g.17387298C>A | CA379770671 | KCNJ11 | c.533G>T (p.Ser178Ile) c.794G>T (p.Ser265Ile) n.952G>T | ClinVar gnomAD |
11 | g.17387298C= | CA1955119202 | KCNJ11 | c.533G= (p.Ser178=) c.794G= (p.Ser265=) n.952G= | |
11 | g.17387298C>G | CA379770674 | KCNJ11 | c.533G>C (p.Ser178Thr) c.794G>C (p.Ser265Thr) n.952G>C | |
11 | g.17387298C>T | CA379770678 | KCNJ11 | c.533G>A (p.Ser178Asn) c.794G>A (p.Ser265Asn) n.952G>A | |
11 | g.17387299T>A | CA379770686 | KCNJ11 | c.532A>T (p.Ser178Cys) c.793A>T (p.Ser265Cys) n.951A>T | |
11 | g.17387299T>C | CA379770689 | KCNJ11 | c.532A>G (p.Ser178Gly) c.793A>G (p.Ser265Gly) n.951A>G | |
11 | g.17387299T>G | CA379770695 | KCNJ11 | c.532A>C (p.Ser178Arg) c.793A>C (p.Ser265Arg) n.951A>C | |
11 | g.17387300G>A | CA473515414 | KCNJ11 | c.531C>T (p.Asn177=) c.792C>T (p.Asn264=) n.950C>T | ClinVar |
11 | g.17387300G>C | CA379770704 | KCNJ11 | c.531C>G (p.Asn177Lys) c.792C>G (p.Asn264Lys) n.950C>G | |
11 | g.17387300G= | CA1955119203 | KCNJ11 | c.531C= (p.Asn177=) c.792C= (p.Asn264=) n.950C= | |
11 | g.17387300G>T | CA379770713 | KCNJ11 | c.531C>A (p.Asn177Lys) c.792C>A (p.Asn264Lys) n.950C>A | |
11 | g.17387301T>A | CA379770716 | KCNJ11 | c.530A>T (p.Asn177Ile) c.791A>T (p.Asn264Ile) n.949A>T | |
11 | g.17387301T>C | CA379770717 | KCNJ11 | c.530A>G (p.Asn177Ser) c.791A>G (p.Asn264Ser) n.949A>G | |
11 | g.17387301T>G | CA379770718 | KCNJ11 | c.530A>C (p.Asn177Thr) c.791A>C (p.Asn264Thr) n.949A>C | |
11 | g.17387302T>A | CA379770721 | KCNJ11 | c.529A>T (p.Asn177Tyr) c.790A>T (p.Asn264Tyr) n.948A>T | |
11 | g.17387302T>C | CA379770723 | KCNJ11 | c.529A>G (p.Asn177Asp) c.790A>G (p.Asn264Asp) n.948A>G | |
11 | g.17387302T>G | CA379770726 | KCNJ11 | c.529A>C (p.Asn177His) c.790A>C (p.Asn264His) n.948A>C | |
11 | g.17387303G>A | CA473515415 | KCNJ11 | c.528C>T (p.Ala176=) c.789C>T (p.Ala263=) n.947C>T | ClinVar |
11 | g.17387303G>C | CA473515416 | KCNJ11 | c.528C>G (p.Ala176=) c.789C>G (p.Ala263=) n.947C>G | |
11 | g.17387303G>T | CA473515417 | KCNJ11 | c.528C>A (p.Ala176=) c.789C>A (p.Ala263=) n.947C>A | |
11 | g.17387304G>A | CA379770731 | KCNJ11 | c.527C>T (p.Ala176Val) c.788C>T (p.Ala263Val) n.946C>T | |
11 | g.17387304G>C | CA379770732 | KCNJ11 | c.527C>G (p.Ala176Gly) c.788C>G (p.Ala263Gly) n.946C>G | |
11 | g.17387304G= | CA1955119204 | KCNJ11 | c.527C= (p.Ala176=) c.788C= (p.Ala263=) n.946C= | |
11 | g.17387304G>T | CA5902247 | KCNJ11 | c.527C>A (p.Ala176Asp) c.788C>A (p.Ala263Asp) n.946C>A | dbSNP ExAC gnomAD |
11 | g.17387305C>A | CA379770734 | KCNJ11 | c.526G>T (p.Ala176Ser) c.787G>T (p.Ala263Ser) n.945G>T | |
11 | g.17387305C>G | CA379770736 | KCNJ11 | c.526G>C (p.Ala176Pro) c.787G>C (p.Ala263Pro) n.945G>C | |
11 | g.17387305C>T | CA379770738 | KCNJ11 | c.526G>A (p.Ala176Thr) c.787G>A (p.Ala263Thr) n.945G>A | |
11 | g.17387306A>C | CA379770746 | KCNJ11 | c.525T>G (p.Asp175Glu) c.786T>G (p.Asp262Glu) n.944T>G | |
11 | g.17387306A>G | CA473515418 | KCNJ11 | c.525T>C (p.Asp175=) c.786T>C (p.Asp262=) n.944T>C | |
11 | g.17387306A>T | CA379770749 | KCNJ11 | c.525T>A (p.Asp175Glu) c.786T>A (p.Asp262Glu) n.944T>A | |
11 | g.17387307T>A | CA379770753 | KCNJ11 | c.524A>T (p.Asp175Val) c.785A>T (p.Asp262Val) n.943A>T | |
11 | g.17387307T>C | CA379770758 | KCNJ11 | c.524A>G (p.Asp175Gly) c.785A>G (p.Asp262Gly) n.943A>G | |
11 | g.17387307T>G | CA379770760 | KCNJ11 | c.524A>C (p.Asp175Ala) c.785A>C (p.Asp262Ala) n.943A>C | |
11 | g.17387308C>A | CA379770762 | KCNJ11 | c.523G>T (p.Asp175Tyr) c.784G>T (p.Asp262Tyr) n.942G>T | |
11 | g.17387308C= | CA1955119205 | KCNJ11 | c.523G= (p.Asp175=) c.784G= (p.Asp262=) n.942G= | |
11 | g.17387308C>G | CA379770764 | KCNJ11 | c.523G>C (p.Asp175His) c.784G>C (p.Asp262His) n.942G>C | |
11 | g.17387308C>T | CA379770767 | KCNJ11 | c.523G>A (p.Asp175Asn) c.784G>A (p.Asp262Asn) n.942G>A | ClinVar |
11 | g.17387309A>C | CA379770770 | KCNJ11 | c.522T>G (p.Ile174Met) c.783T>G (p.Ile261Met) n.941T>G | |
11 | g.17387309A>G | CA473515420 | KCNJ11 | c.522T>C (p.Ile174=) c.783T>C (p.Ile261=) n.941T>C | |
11 | g.17387309A>T | CA473515419 | KCNJ11 | c.522T>A (p.Ile174=) c.783T>A (p.Ile261=) n.941T>A | |
11 | g.17387310A= | CA1955119206 | KCNJ11 | c.521T= (p.Ile174=) c.782T= (p.Ile261=) n.940T= | |
11 | g.17387310A>C | CA379770775 | KCNJ11 | c.521T>G (p.Ile174Ser) c.782T>G (p.Ile261Ser) n.940T>G | |
11 | g.17387310A>G | CA379770793 | KCNJ11 | c.521T>C (p.Ile174Thr) c.782T>C (p.Ile261Thr) n.940T>C |