Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
10 | g.80274599C>A | CA377360416 | MAT1A | c.1006G>T (p.Gly336Ter) n.238G>T n.518G>T c.883G>T (p.Gly295Ter) | |
10 | g.80274599C= | CA1922577912 | MAT1A | c.1006G= (p.Gly336=) n.238G= n.518G= c.883G= (p.Gly295=) | |
10 | g.80274599C>G | CA377360417 | MAT1A | c.1006G>C (p.Gly336Arg) n.238G>C n.518G>C c.883G>C (p.Gly295Arg) | |
10 | g.80274599C>T | CA114842 | MAT1A | c.1006G>A (p.Gly336Arg) n.238G>A n.518G>A c.883G>A (p.Gly295Arg) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
10 | g.80274600G>A | CA5576636 | MAT1A | c.1005C>T (p.Tyr335=) n.237C>T n.517C>T c.882C>T (p.Tyr294=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
10 | g.80274600G>C | CA377360418 | MAT1A | c.1005C>G (p.Tyr335Ter) n.237C>G n.517C>G c.882C>G (p.Tyr294Ter) | |
10 | g.80274600G= | CA1922577915 | MAT1A | c.1005C= (p.Tyr335=) n.237C= n.517C= c.882C= (p.Tyr294=) | |
10 | g.80274600G>T | CA377360419 | MAT1A | c.1005C>A (p.Tyr335Ter) n.237C>A n.517C>A c.882C>A (p.Tyr294Ter) | |
10 | g.80274601T>A | CA377360420 | MAT1A | c.1004A>T (p.Tyr335Phe) n.236A>T n.516A>T c.881A>T (p.Tyr294Phe) | |
10 | g.80274601T>C | CA377360422 | MAT1A | c.1004A>G (p.Tyr335Cys) n.236A>G n.516A>G c.881A>G (p.Tyr294Cys) | gnomAD v4 |
10 | g.80274601T>G | CA377360421 | MAT1A | c.1004A>C (p.Tyr335Ser) n.236A>C n.516A>C c.881A>C (p.Tyr294Ser) | |
10 | g.80274602A= | CA1922577918 | MAT1A | c.1003T= (p.Tyr335=) n.235T= n.515T= c.880T= (p.Tyr294=) | |
10 | g.80274602A>C | CA377360423 | MAT1A | c.1003T>G (p.Tyr335Asp) n.235T>G n.515T>G c.880T>G (p.Tyr294Asp) | |
10 | g.80274602A>G | CA5576637 | MAT1A | c.1003T>C (p.Tyr335His) n.235T>C n.515T>C c.880T>C (p.Tyr294His) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
10 | g.80274602A>T | CA377360424 | MAT1A | c.1003T>A (p.Tyr335Asn) n.235T>A n.515T>A c.880T>A (p.Tyr294Asn) | |
10 | g.80274603G>A | CA5576638 | MAT1A | c.1002C>T (p.Thr334=) n.234C>T n.514C>T c.879C>T (p.Thr293=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
10 | g.80274603G>C | CA470467259 | MAT1A | c.1002C>G (p.Thr334=) n.234C>G n.514C>G c.879C>G (p.Thr293=) | |
10 | g.80274603G= | CA1922577920 | MAT1A | c.1002C= (p.Thr334=) n.234C= n.514C= c.879C= (p.Thr293=) | |
10 | g.80274603G>T | CA470467260 | MAT1A | c.1002C>A (p.Thr334=) n.234C>A n.514C>A c.879C>A (p.Thr293=) | COSMIC |
10 | g.80274604G>A | CA377360425 | MAT1A | c.1001C>T (p.Thr334Ile) n.233C>T n.513C>T c.878C>T (p.Thr293Ile) | |
10 | g.80274604G>C | CA377360426 | MAT1A | c.1001C>G (p.Thr334Ser) n.233C>G n.513C>G c.878C>G (p.Thr293Ser) | |
10 | g.80274604G>T | CA377360427 | MAT1A | c.1001C>A (p.Thr334Asn) n.233C>A n.513C>A c.878C>A (p.Thr293Asn) | |
10 | g.80274605T>A | CA377360428 | MAT1A | c.1000A>T (p.Thr334Ser) n.232A>T n.512A>T c.877A>T (p.Thr293Ser) | |
10 | g.80274605T>C | CA5576639 | MAT1A | c.1000A>G (p.Thr334Ala) n.232A>G n.512A>G c.877A>G (p.Thr293Ala) | dbSNP ExAC |
10 | g.80274605T>G | CA377360429 | MAT1A | c.1000A>C (p.Thr334Pro) n.232A>C n.512A>C c.877A>C (p.Thr293Pro) | |
10 | g.80274605T= | CA1922577921 | MAT1A | c.1000A= (p.Thr334=) n.232A= n.512A= c.877A= (p.Thr293=) | |
10 | g.80274606G>A | CA470467261 | MAT1A | c.999C>T (p.Phe333=) n.231C>T n.511C>T c.876C>T (p.Phe292=) | gnomAD v4 |
10 | g.80274606G>C | CA377360431 | MAT1A | c.999C>G (p.Phe333Leu) n.231C>G n.511C>G c.876C>G (p.Phe292Leu) | |
10 | g.80274606G>T | CA377360430 | MAT1A | c.999C>A (p.Phe333Leu) n.231C>A n.511C>A c.876C>A (p.Phe292Leu) | |
10 | g.80274607A>C | CA377360432 | MAT1A | c.998T>G (p.Phe333Cys) n.230T>G n.510T>G c.875T>G (p.Phe292Cys) | |
10 | g.80274607A>G | CA377360433 | MAT1A | c.998T>C (p.Phe333Ser) n.230T>C n.510T>C c.875T>C (p.Phe292Ser) | |
10 | g.80274607A>T | CA377360434 | MAT1A | c.998T>A (p.Phe333Tyr) n.230T>A n.510T>A c.875T>A (p.Phe292Tyr) | |
10 | g.80274608A>C | CA377360435 | MAT1A | c.997T>G (p.Phe333Val) n.229T>G n.509T>G c.874T>G (p.Phe292Val) | COSMIC |
10 | g.80274608A>G | CA377360436 | MAT1A | c.997T>C (p.Phe333Leu) n.229T>C n.509T>C c.874T>C (p.Phe292Leu) | |
10 | g.80274608A>T | CA377360437 | MAT1A | c.997T>A (p.Phe333Ile) n.229T>A n.509T>A c.874T>A (p.Phe292Ile) | |
10 | g.80274609G>A | CA5576640 | MAT1A | c.996C>T (p.Ile332=) n.228C>T n.508C>T c.873C>T (p.Ile291=) | dbSNP ExAC gnomAD v2 gnomAD v4 |
10 | g.80274609G>C | CA377360438 | MAT1A | c.996C>G (p.Ile332Met) n.228C>G n.508C>G c.873C>G (p.Ile291Met) | |
10 | g.80274609G= | CA1922572892 | MAT1A | c.996C= (p.Ile332=) n.228C= n.508C= c.873C= (p.Ile291=) | |
10 | g.80274609G>T | CA470467262 | MAT1A | c.996C>A (p.Ile332=) n.228C>A n.508C>A c.873C>A (p.Ile291=) | |
10 | g.80274610A>C | CA377360439 | MAT1A | c.995T>G (p.Ile332Ser) n.227T>G n.507T>G c.872T>G (p.Ile291Ser) | |
10 | g.80274610A>G | CA377360440 | MAT1A | c.995T>C (p.Ile332Thr) n.227T>C n.507T>C c.872T>C (p.Ile291Thr) | |
10 | g.80274610A>T | CA377360441 | MAT1A | c.995T>A (p.Ile332Asn) n.227T>A n.507T>A c.872T>A (p.Ile291Asn) | |
10 | g.80274611T>A | CA377360442 | MAT1A | c.994A>T (p.Ile332Phe) n.226A>T n.506A>T c.871A>T (p.Ile291Phe) | |
10 | g.80274611T>C | CA377360443 | MAT1A | c.994A>G (p.Ile332Val) n.226A>G n.506A>G c.871A>G (p.Ile291Val) | |
10 | g.80274611T>G | CA377360444 | MAT1A | c.994A>C (p.Ile332Leu) n.226A>C n.506A>C c.871A>C (p.Ile291Leu) | |
10 | g.80274612G>A | CA470467263 | MAT1A | c.993C>T (p.Ser331=) n.225C>T n.505C>T c.870C>T (p.Ser290=) | dbSNP gnomAD v2 COSMIC |
10 | g.80274612G>C | CA470467264 | MAT1A | c.993C>G (p.Ser331=) n.225C>G n.505C>G c.870C>G (p.Ser290=) | |
10 | g.80274612G= | CA1922572894 | MAT1A | c.993C= (p.Ser331=) n.225C= n.505C= c.870C= (p.Ser290=) | |
10 | g.80274612G>T | CA470467265 | MAT1A | c.993C>A (p.Ser331=) n.225C>A n.505C>A c.870C>A (p.Ser290=) | |
10 | g.80274613G>A | CA377360445 | MAT1A | c.992C>T (p.Ser331Phe) n.224C>T n.504C>T c.869C>T (p.Ser290Phe) | COSMIC |