Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
6 | g.49451568_49451570del | CA1627389324 | MMUT | c.1233_1235del (p.Ile412del) | ClinVar dbSNP |
6 | g.49451565_49451570del | CA2499218330 | MMUT | c.1230_1235del (p.Ile411_Ile412del) | ClinVar dbSNP |
6 | g.49451568G>A | CA450606394 | MMUT | c.1230C>T (p.Ile410=) | |
6 | g.49451568G>C | CA364398843 | MMUT | c.1230C>G (p.Ile410Met) | |
6 | g.49451568G>T | CA450606391 | MMUT | c.1230C>A (p.Ile410=) | |
6 | g.49451569A>C | CA364398844 | MMUT | c.1229T>G (p.Ile410Ser) | |
6 | g.49451569A>G | CA364398845 | MMUT | c.1229T>C (p.Ile410Thr) | |
6 | g.49451569A>T | CA364398846 | MMUT | c.1229T>A (p.Ile410Asn) | |
6 | g.49451570T>A | CA364398849 | MMUT | c.1228A>T (p.Ile410Phe) | |
6 | g.49451570T>C | CA364398847 | MMUT | c.1228A>G (p.Ile410Val) | |
6 | g.49451570T>G | CA364398848 | MMUT | c.1228A>C (p.Ile410Leu) | |
6 | g.49451571T>A | CA364398850 | MMUT | c.1227A>T (p.Gln409His) | |
6 | g.49451571T>C | CA450606402 | MMUT | c.1227A>G (p.Gln409=) | |
6 | g.49451571T>G | CA364398851 | MMUT | c.1227A>C (p.Gln409His) | |
6 | g.49451572T>A | CA364398852 | MMUT | c.1226A>T (p.Gln409Leu) | |
6 | g.49451572T>C | CA364398853 | MMUT | c.1226A>G (p.Gln409Arg) | |
6 | g.49451572T>G | CA364398854 | MMUT | c.1226A>C (p.Gln409Pro) | |
6 | g.49451573G>A | CA364398855 | MMUT | c.1225C>T (p.Gln409Ter) | gnomAD v4 |
6 | g.49451573G>C | CA364398857 | MMUT | c.1225C>G (p.Gln409Glu) | |
6 | g.49451573G>T | CA364398856 | MMUT | c.1225C>A (p.Gln409Lys) | |
6 | g.49451574T>A | CA450606411 | MMUT | c.1224A>T (p.Thr408=) | |
6 | g.49451574T>C | CA450606413 | MMUT | c.1224A>G (p.Thr408=) | gnomAD v4 |
6 | g.49451574T>G | CA450606412 | MMUT | c.1224A>C (p.Thr408=) | |
6 | g.49451575G>A | CA364398858 | MMUT | c.1223C>T (p.Thr408Ile) | gnomAD v4 |
6 | g.49451575G>C | CA364398859 | MMUT | c.1223C>G (p.Thr408Arg) | |
6 | g.49451575G>T | CA364398860 | MMUT | c.1223C>A (p.Thr408Lys) | |
6 | g.49451576T>A | CA3846937 | MMUT | c.1222A>T (p.Thr408Ser) | dbSNP ExAC gnomAD v2 gnomAD v4 |
6 | g.49451576T>C | CA364398861 | MMUT | c.1222A>G (p.Thr408Ala) | |
6 | g.49451576T>G | CA364398862 | MMUT | c.1222A>C (p.Thr408Pro) | |
6 | g.49451576T= | CA1627389327 | MMUT | c.1222A= (p.Thr408=) | |
6 | g.49451577G>A | CA450606421 | MMUT | c.1221C>T (p.Asn407=) | |
6 | g.49451577G>C | CA364398863 | MMUT | c.1221C>G (p.Asn407Lys) | |
6 | g.49451577G>T | CA364398864 | MMUT | c.1221C>A (p.Asn407Lys) | |
6 | g.49451578T>A | CA364398865 | MMUT | c.1220A>T (p.Asn407Ile) | |
6 | g.49451578T>C | CA3846938 | MMUT | c.1220A>G (p.Asn407Ser) | dbSNP ExAC gnomAD v2 gnomAD v4 |
6 | g.49451578T>G | CA364398866 | MMUT | c.1220A>C (p.Asn407Thr) | |
6 | g.49451578T= | CA1627389328 | MMUT | c.1220A= (p.Asn407=) | |
6 | g.49451579T>A | CA3846939 | MMUT | c.1219A>T (p.Asn407Tyr) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
6 | g.49451579T>C | CA364398868 | MMUT | c.1219A>G (p.Asn407Asp) | |
6 | g.49451579T>G | CA364398867 | MMUT | c.1219A>C (p.Asn407His) | |
6 | g.49451579T= | CA1627389330 | MMUT | c.1219A= (p.Asn407=) | |
6 | g.49451579_49451580delinsTC | CA1627389329 | MMUT | c.1218_1219delinsGA (p.Arg406=) | |
6 | g.49451580C>A | CA364398869 | MMUT | c.1218G>T (p.Arg406Ser) | |
6 | g.49451580C>G | CA364398870 | MMUT | c.1218G>C (p.Arg406Ser) | |
6 | g.49451580C>T | CA450606432 | MMUT | c.1218G>A (p.Arg406=) | |
6 | g.49451581del | CA138796356 | MMUT | c.1218del (p.Asn407ThrfsTer24) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
6 | g.49451581C>A | CA364398871 | MMUT | c.1217G>T (p.Arg406Met) | |
6 | g.49451581C>G | CA364398872 | MMUT | c.1217G>C (p.Arg406Thr) | |
6 | g.49451581C>T | CA364398873 | MMUT | c.1217G>A (p.Arg406Lys) | COSMIC |
6 | g.49451582T>A | CA364398874 | MMUT | c.1216A>T (p.Arg406Trp) |