Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
8 | g.132908189C>A | CA372243769 | TG | c.3851C>A (p.Pro1284His) c.506C>A c.3590C>A (p.Pro1197His) | |
8 | g.132908189C>G | CA372243767 | TG | c.3851C>G (p.Pro1284Arg) c.506C>G c.3590C>G (p.Pro1197Arg) | |
8 | g.132908189C>T | CA372243766 | TG | c.3851C>T (p.Pro1284Leu) c.506C>T c.3590C>T (p.Pro1197Leu) | gnomAD v4 |
8 | g.132908190C>A | CA463011513 | TG | c.3852C>A (p.Pro1284=) c.507C>A c.3591C>A (p.Pro1197=) | |
8 | g.132908190C= | CA1821000199 | TG | c.3852C= (p.Pro1284=) c.507C= c.3591C= (p.Pro1197=) | |
8 | g.132908190C>G | CA4883929 | TG | c.3852C>G (p.Pro1284=) c.507C>G c.3591C>G (p.Pro1197=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
8 | g.132908190C>T | CA463011516 | TG | c.3852C>T (p.Pro1284=) c.507C>T c.3591C>T (p.Pro1197=) | dbSNP gnomAD v2 |
8 | g.132908191C>A | CA372243771 | TG | c.3853C>A (p.Gln1285Lys) c.508C>A c.3592C>A (p.Gln1198Lys) | dbSNP gnomAD v3 gnomAD v4 |
8 | g.132908191C= | CA1821000200 | TG | c.3853C= (p.Gln1285=) c.508C= c.3592C= (p.Gln1198=) | |
8 | g.132908191C>G | CA372243772 | TG | c.3853C>G (p.Gln1285Glu) c.508C>G c.3592C>G (p.Gln1198Glu) | |
8 | g.132908191C>T | CA372243774 | TG | c.3853C>T (p.Gln1285Ter) c.508C>T c.3592C>T (p.Gln1198Ter) | |
8 | g.132908192A= | CA1821000201 | TG | c.3854A= (p.Gln1285=) c.509A= c.3593A= (p.Gln1198=) | |
8 | g.132908192A>C | CA372243776 | TG | c.3854A>C (p.Gln1285Pro) c.509A>C c.3593A>C (p.Gln1198Pro) | gnomAD v4 |
8 | g.132908192A>G | CA372243778 | TG | c.3854A>G (p.Gln1285Arg) c.509A>G c.3593A>G (p.Gln1198Arg) | dbSNP gnomAD v3 gnomAD v4 |
8 | g.132908192A>T | CA372243779 | TG | c.3854A>T (p.Gln1285Leu) c.509A>T c.3593A>T (p.Gln1198Leu) | |
8 | g.132908193G>A | CA463011526 | TG | c.3855G>A (p.Gln1285=) c.510G>A c.3594G>A (p.Gln1198=) | COSMIC |
8 | g.132908193G>C | CA372243780 | TG | c.3855G>C (p.Gln1285His) c.510G>C c.3594G>C (p.Gln1198His) | |
8 | g.132908193G= | CA1821000202 | TG | c.3855G= (p.Gln1285=) c.510G= c.3594G= (p.Gln1198=) | |
8 | g.132908193G>T | CA372243783 | TG | c.3855G>T (p.Gln1285His) c.510G>T c.3594G>T (p.Gln1198His) | dbSNP gnomAD v3 gnomAD v4 |
8 | g.132908194C>A | CA16618602 | TG | c.3856C>A (p.Leu1286Met) c.511C>A c.3595C>A (p.Leu1199Met) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
8 | g.132908194C= | CA1821000203 | TG | c.3856C= (p.Leu1286=) c.511C= c.3595C= (p.Leu1199=) | |
8 | g.132908194C>G | CA372243785 | TG | c.3856C>G (p.Leu1286Val) c.511C>G c.3595C>G (p.Leu1199Val) | gnomAD v4 |
8 | g.132908194C>T | CA463011532 | TG | c.3856C>T (p.Leu1286=) c.511C>T c.3595C>T (p.Leu1199=) | |
8 | g.132908195T>A | CA372243787 | TG | c.3857T>A (p.Leu1286Gln) c.512T>A c.3596T>A (p.Leu1199Gln) | |
8 | g.132908195T>C | CA372243789 | TG | c.3857T>C (p.Leu1286Pro) c.512T>C c.3596T>C (p.Leu1199Pro) | |
8 | g.132908195T>G | CA372243791 | TG | c.3857T>G (p.Leu1286Arg) c.512T>G c.3596T>G (p.Leu1199Arg) | |
8 | g.132908196G>A | CA463011539 | TG | c.3858G>A (p.Leu1286=) c.513G>A c.3597G>A (p.Leu1199=) | gnomAD v4 |
8 | g.132908196G>C | CA463011540 | TG | c.3858G>C (p.Leu1286=) c.513G>C c.3597G>C (p.Leu1199=) | |
8 | g.132908196G>T | CA463011542 | TG | c.3858G>T (p.Leu1286=) c.513G>T c.3597G>T (p.Leu1199=) | |
8 | g.132908197T>A | CA372243795 | TG | c.3859T>A (p.Trp1287Arg) c.514T>A c.3598T>A (p.Trp1200Arg) | |
8 | g.132908197T>C | CA372243797 | TG | c.3859T>C (p.Trp1287Arg) c.514T>C c.3598T>C (p.Trp1200Arg) | |
8 | g.132908197T>G | CA372243793 | TG | c.3859T>G (p.Trp1287Gly) c.514T>G c.3598T>G (p.Trp1200Gly) | |
8 | g.132908198G>A | CA372243798 | TG | c.3860G>A (p.Trp1287Ter) c.515G>A c.3599G>A (p.Trp1200Ter) | |
8 | g.132908198G>C | CA372243799 | TG | c.3860G>C (p.Trp1287Ser) c.515G>C c.3599G>C (p.Trp1200Ser) | |
8 | g.132908198G>T | CA372243800 | TG | c.3860G>T (p.Trp1287Leu) c.515G>T c.3599G>T (p.Trp1200Leu) | gnomAD v4 |
8 | g.132908199G>A | CA372243801 | TG | c.3861G>A (p.Trp1287Ter) c.516G>A c.3600G>A (p.Trp1200Ter) | gnomAD v4 |
8 | g.132908199G>C | CA372243802 | TG | c.3861G>C (p.Trp1287Cys) c.516G>C c.3600G>C (p.Trp1200Cys) | |
8 | g.132908199G>T | CA372243803 | TG | c.3861G>T (p.Trp1287Cys) c.516G>T c.3600G>T (p.Trp1200Cys) | gnomAD v4 |
8 | g.132908200C>A | CA372243806 | TG | c.3862C>A (p.Gln1288Lys) c.517C>A c.3601C>A (p.Gln1201Lys) | dbSNP |
8 | g.132908200C= | CA1821000204 | TG | c.3862C= (p.Gln1288=) c.517C= c.3601C= (p.Gln1201=) | |
8 | g.132908200C>G | CA372243804 | TG | c.3862C>G (p.Gln1288Glu) c.517C>G c.3601C>G (p.Gln1201Glu) | |
8 | g.132908200C>T | CA372243805 | TG | c.3862C>T (p.Gln1288Ter) c.517C>T c.3601C>T (p.Gln1201Ter) | |
8 | g.132908201A>C | CA372243807 | TG | c.3863A>C (p.Gln1288Pro) c.518A>C c.3602A>C (p.Gln1201Pro) | |
8 | g.132908201A>G | CA372243808 | TG | c.3863A>G (p.Gln1288Arg) c.518A>G c.3602A>G (p.Gln1201Arg) | gnomAD v4 |
8 | g.132908201A>T | CA372243809 | TG | c.3863A>T (p.Gln1288Leu) c.518A>T c.3602A>T (p.Gln1201Leu) | |
8 | g.132908202G>A | CA463011564 | TG | c.3864G>A (p.Gln1288=) c.519G>A c.3603G>A (p.Gln1201=) | |
8 | g.132908202G>C | CA372243810 | TG | c.3864G>C (p.Gln1288His) c.519G>C c.3603G>C (p.Gln1201His) | |
8 | g.132908202G>T | CA372243811 | TG | c.3864G>T (p.Gln1288His) c.519G>T c.3603G>T (p.Gln1201His) | gnomAD v4 |
8 | g.132908203A= | CA1821000205 | TG | c.3865A= (p.Thr1289=) c.520A= c.3604A= (p.Thr1202=) | |
8 | g.132908203A>C | CA372243812 | TG | c.3865A>C (p.Thr1289Pro) c.520A>C c.3604A>C (p.Thr1202Pro) |