Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
11 | g.2159842_2161516del | CA344912 | |||
11 | g.2160809G>A | CA123087 | INS,INS-IGF2 | c.163C>T (p.Arg55Cys) n.222C>T | ClinVar dbSNP gnomAD v2 |
11 | g.2160809G>C | CA379121353 | INS,INS-IGF2 | c.163C>G (p.Arg55Gly) n.222C>G | |
11 | g.2160809G= | CA1948026988 | INS,INS-IGF2 | c.163C= (p.Arg55=) n.222C= | |
11 | g.2160809G>T | CA379121351 | INS,INS-IGF2 | c.163C>A (p.Arg55Ser) n.222C>A | |
11 | g.2160810G>A | CA5818179 | INS,INS-IGF2 | c.162C>T (p.Thr54=) n.221C>T | dbSNP ExAC gnomAD v2 gnomAD v4 |
11 | g.2160810G>C | CA472031759 | INS,INS-IGF2 | c.162C>G (p.Thr54=) n.221C>G | gnomAD v4 |
11 | g.2160810G= | CA1948026989 | INS,INS-IGF2 | c.162C= (p.Thr54=) n.221C= | |
11 | g.2160810G>T | CA472031761 | INS,INS-IGF2 | c.162C>A (p.Thr54=) n.221C>A | dbSNP |
11 | g.2160811G>A | CA379121361 | INS,INS-IGF2 | c.161C>T (p.Thr54Ile) n.220C>T | |
11 | g.2160811G>C | CA379121362 | INS,INS-IGF2 | c.161C>G (p.Thr54Ser) n.220C>G | dbSNP gnomAD v4 |
11 | g.2160811G= | CA1948026990 | INS,INS-IGF2 | c.161C= (p.Thr54=) n.220C= | |
11 | g.2160811G>T | CA379121363 | INS,INS-IGF2 | c.161C>A (p.Thr54Asn) n.220C>A | |
11 | g.2160812T>A | CA379121366 | INS,INS-IGF2 | c.160A>T (p.Thr54Ser) n.219A>T | dbSNP |
11 | g.2160812T>C | CA379121374 | INS,INS-IGF2 | c.160A>G (p.Thr54Ala) n.219A>G | |
11 | g.2160812T>G | CA379121380 | INS,INS-IGF2 | c.160A>C (p.Thr54Pro) n.219A>C | dbSNP |
11 | g.2160812T= | CA1948026991 | INS,INS-IGF2 | c.160A= (p.Thr54=) n.219A= | |
11 | g.2160813C>A | CA379121385 | INS,INS-IGF2 | c.159G>T (p.Lys53Asn) n.218G>T | |
11 | g.2160813C>G | CA379121387 | INS,INS-IGF2 | c.159G>C (p.Lys53Asn) n.218G>C | |
11 | g.2160813C>T | CA472031770 | INS,INS-IGF2 | c.159G>A (p.Lys53=) n.218G>A | COSMIC COSMIC |
11 | g.2160814T>A | CA379121389 | INS,INS-IGF2 | c.158A>T (p.Lys53Met) n.217A>T | |
11 | g.2160814T>C | CA379121393 | INS,INS-IGF2 | c.158A>G (p.Lys53Arg) n.217A>G | |
11 | g.2160814T>G | CA5818180 | INS,INS-IGF2 | c.158A>C (p.Lys53Thr) n.217A>C | dbSNP ExAC gnomAD v3 gnomAD v4 |
11 | g.2160814T= | CA1948026992 | INS,INS-IGF2 | c.158A= (p.Lys53=) n.217A= | |
11 | g.2160815T>A | CA379121402 | INS,INS-IGF2 | c.157A>T (p.Lys53Ter) n.216A>T | |
11 | g.2160815T>C | CA5818181 | INS,INS-IGF2 | c.157A>G (p.Lys53Glu) n.216A>G | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
11 | g.2160815T>G | CA379121398 | INS,INS-IGF2 | c.157A>C (p.Lys53Gln) n.216A>C | |
11 | g.2160815T= | CA1948026993 | INS,INS-IGF2 | c.157A= (p.Lys53=) n.216A= | |
11 | g.2160816G>A | CA472031777 | INS,INS-IGF2 | c.156C>T (p.Pro52=) n.215C>T | |
11 | g.2160816G>C | CA216276321 | INS,INS-IGF2 | c.156C>G (p.Pro52=) n.215C>G | dbSNP gnomAD v3 gnomAD v4 |
11 | g.2160816G= | CA1948026995 | INS,INS-IGF2 | c.156C= (p.Pro52=) n.215C= | |
11 | g.2160816G>T | CA472031780 | INS,INS-IGF2 | c.156C>A (p.Pro52=) n.215C>A | gnomAD v4 |
11 | g.2160817G>A | CA379121407 | INS,INS-IGF2 | c.155C>T (p.Pro52Leu) n.214C>T | ClinVar dbSNP |
11 | g.2160817G>C | CA5818182 | INS,INS-IGF2 | c.155C>G (p.Pro52Arg) n.214C>G | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
11 | g.2160817G= | CA1948026996 | INS,INS-IGF2 | c.155C= (p.Pro52=) n.214C= | |
11 | g.2160817G>T | CA379121410 | INS,INS-IGF2 | c.155C>A (p.Pro52His) n.214C>A | ClinVar dbSNP |
11 | g.2160818G>A | CA379121418 | INS,INS-IGF2 | c.154C>T (p.Pro52Ser) n.213C>T | dbSNP gnomAD v4 |
11 | g.2160818G>C | CA379121425 | INS,INS-IGF2 | c.154C>G (p.Pro52Ala) n.213C>G | |
11 | g.2160818G= | CA1948026999 | INS,INS-IGF2 | c.154C= (p.Pro52=) n.213C= | |
11 | g.2160818G>T | CA379121422 | INS,INS-IGF2 | c.154C>A (p.Pro52Thr) n.213C>A | dbSNP gnomAD v2 gnomAD v4 |
11 | g.2160819T>A | CA472031787 | INS,INS-IGF2 | c.153A>T (p.Thr51=) n.212A>T | |
11 | g.2160819T>C | CA5818184 | INS,INS-IGF2 | c.153A>G (p.Thr51=) n.212A>G | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
11 | g.2160819T>G | CA5818183 | INS,INS-IGF2 | c.153A>C (p.Thr51=) n.212A>C | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
11 | g.2160819T= | CA1948027000 | INS,INS-IGF2 | c.153A= (p.Thr51=) n.212A= | |
11 | g.2160820G>A | CA5818185 | INS,INS-IGF2 | c.152C>T (p.Thr51Ile) n.211C>T | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
11 | g.2160820G>C | CA379121435 | INS,INS-IGF2 | c.152C>G (p.Thr51Arg) n.211C>G | |
11 | g.2160820G= | CA1948027002 | INS,INS-IGF2 | c.152C= (p.Thr51=) n.211C= | |
11 | g.2160820G>T | CA379121442 | INS,INS-IGF2 | c.152C>A (p.Thr51Lys) n.211C>A | |
11 | g.2160821T>A | CA379121446 | INS,INS-IGF2 | c.151A>T (p.Thr51Ser) n.210A>T | |
11 | g.2160821T>C | CA379121449 | INS,INS-IGF2 | c.151A>G (p.Thr51Ala) n.210A>G | dbSNP gnomAD v2 gnomAD v4 |