Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
9 | g.127814982_127820052del | CA1139659920 | ClinVar | ||
9 | g.127815975G>A | CA374971866 | ENG | c.1274C>T (p.Thr425Ile) c.1820C>T (p.Thr607Ile) | gnomAD v4 |
9 | g.127815975G>C | CA374971870 | ENG | c.1274C>G (p.Thr425Ser) c.1820C>G (p.Thr607Ser) | |
9 | g.127815975G>T | CA374971878 | ENG | c.1274C>A (p.Thr425Asn) c.1820C>A (p.Thr607Asn) | |
9 | g.127815976T>A | CA374971883 | ENG | c.1273A>T (p.Thr425Ser) c.1819A>T (p.Thr607Ser) | |
9 | g.127815976T>C | CA374971885 | ENG | c.1273A>G (p.Thr425Ala) c.1819A>G (p.Thr607Ala) | COSMIC COSMIC |
9 | g.127815976T>G | CA374971888 | ENG | c.1273A>C (p.Thr425Pro) c.1819A>C (p.Thr607Pro) | |
9 | g.127815977G>A | CA467474382 | ENG | c.1272C>T (p.Leu424=) c.1818C>T (p.Leu606=) | |
9 | g.127815977G>C | CA467474383 | ENG | c.1272C>G (p.Leu424=) c.1818C>G (p.Leu606=) | |
9 | g.127815977G= | CA1879981828 | ENG | c.1272C= (p.Leu424=) c.1818C= (p.Leu606=) | |
9 | g.127815977G>T | CA467474384 | ENG | c.1272C>A (p.Leu424=) c.1818C>A (p.Leu606=) | ClinVar dbSNP gnomAD v4 |
9 | g.127815978A>C | CA374971895 | ENG | c.1271T>G (p.Leu424Arg) c.1817T>G (p.Leu606Arg) | |
9 | g.127815978A>G | CA374971914 | ENG | c.1271T>C (p.Leu424Pro) c.1817T>C (p.Leu606Pro) | |
9 | g.127815978A>T | CA374971899 | ENG | c.1271T>A (p.Leu424His) c.1817T>A (p.Leu606His) | |
9 | g.127815979G>A | CA374971917 | ENG | c.1270C>T (p.Leu424Phe) c.1816C>T (p.Leu606Phe) | dbSNP gnomAD v2 gnomAD v4 |
9 | g.127815979G>C | CA374971918 | ENG | c.1270C>G (p.Leu424Val) c.1816C>G (p.Leu606Val) | |
9 | g.127815979G= | CA1879981833 | ENG | c.1270C= (p.Leu424=) c.1816C= (p.Leu606=) | |
9 | g.127815979G>T | CA374971922 | ENG | c.1270C>A (p.Leu424Ile) c.1816C>A (p.Leu606Ile) | gnomAD v4 |
9 | g.127815980C>A | CA467474387 | ENG | c.1269G>T (p.Leu423=) c.1815G>T (p.Leu605=) | |
9 | g.127815980C>G | CA467474389 | ENG | c.1269G>C (p.Leu423=) c.1815G>C (p.Leu605=) | |
9 | g.127815980C>T | CA467474391 | ENG | c.1269G>A (p.Leu423=) c.1815G>A (p.Leu605=) | ClinVar dbSNP gnomAD v4 |
9 | g.127815981A>C | CA374971935 | ENG | c.1268T>G (p.Leu423Arg) c.1814T>G (p.Leu605Arg) | |
9 | g.127815981A>G | CA374971943 | ENG | c.1268T>C (p.Leu423Pro) c.1814T>C (p.Leu605Pro) | gnomAD v4 |
9 | g.127815981A>T | CA374971945 | ENG | c.1268T>A (p.Leu423Gln) c.1814T>A (p.Leu605Gln) | |
9 | g.127815982G>A | CA467474393 | ENG | c.1267C>T (p.Leu423=) c.1813C>T (p.Leu605=) | |
9 | g.127815982G>C | CA374971948 | ENG | c.1267C>G (p.Leu423Val) c.1813C>G (p.Leu605Val) | |
9 | g.127815982G>T | CA374971953 | ENG | c.1267C>A (p.Leu423Met) c.1813C>A (p.Leu605Met) | |
9 | g.127815983G>A | CA467474395 | ENG | c.1266C>T (p.Ala422=) c.1812C>T (p.Ala604=) | |
9 | g.127815983G>C | CA467474396 | ENG | c.1266C>G (p.Ala422=) c.1812C>G (p.Ala604=) | |
9 | g.127815983G>T | CA467474397 | ENG | c.1266C>A (p.Ala422=) c.1812C>A (p.Ala604=) | gnomAD v4 |
9 | g.127815984G>A | CA374971968 | ENG | c.1265C>T (p.Ala422Val) c.1811C>T (p.Ala604Val) | dbSNP gnomAD v4 |
9 | g.127815984G>C | CA374971969 | ENG | c.1265C>G (p.Ala422Gly) c.1811C>G (p.Ala604Gly) | |
9 | g.127815984G= | CA1879981839 | ENG | c.1265C= (p.Ala422=) c.1811C= (p.Ala604=) | |
9 | g.127815984G>T | CA374971970 | ENG | c.1265C>A (p.Ala422Asp) c.1811C>A (p.Ala604Asp) | gnomAD v4 |
9 | g.127815985C>A | CA374971974 | ENG | c.1264G>T (p.Ala422Ser) c.1810G>T (p.Ala604Ser) | gnomAD v4 |
9 | g.127815985C>G | CA374971971 | ENG | c.1264G>C (p.Ala422Pro) c.1810G>C (p.Ala604Pro) | |
9 | g.127815985C>T | CA374971973 | ENG | c.1264G>A (p.Ala422Thr) c.1810G>A (p.Ala604Thr) | gnomAD v4 |
9 | g.127815986C>A | CA467474405 | ENG | c.1263G>T (p.Gly421=) c.1809G>T (p.Gly603=) | |
9 | g.127815986C>G | CA467474408 | ENG | c.1263G>C (p.Gly421=) c.1809G>C (p.Gly603=) | |
9 | g.127815986C>T | CA467474407 | ENG | c.1263G>A (p.Gly421=) c.1809G>A (p.Gly603=) | gnomAD v4 |
9 | g.127815987C>A | CA374971975 | ENG | c.1262G>T (p.Gly421Val) c.1808G>T (p.Gly603Val) | gnomAD v4 |
9 | g.127815987C= | CA1879981843 | ENG | c.1262G= (p.Gly421=) c.1808G= (p.Gly603=) | |
9 | g.127815987C>G | CA374971977 | ENG | c.1262G>C (p.Gly421Ala) c.1808G>C (p.Gly603Ala) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
9 | g.127815987C>T | CA374971978 | ENG | c.1262G>A (p.Gly421Glu) c.1808G>A (p.Gly603Glu) | |
9 | g.127815988C>A | CA374971980 | ENG | c.1261G>T (p.Gly421Trp) c.1807G>T (p.Gly603Trp) | |
9 | g.127815988C= | CA1879981849 | ENG | c.1261G= (p.Gly421=) c.1807G= (p.Gly603=) | |
9 | g.127815988C>G | CA374971981 | ENG | c.1261G>C (p.Gly421Arg) c.1807G>C (p.Gly603Arg) | |
9 | g.127815988C>T | CA374971982 | ENG | c.1261G>A (p.Gly421Arg) c.1807G>A (p.Gly603Arg) | ClinVar dbSNP gnomAD v4 |
9 | g.127815989G>A | CA5252624 | ENG | c.1260C>T (p.Ile420=) c.1806C>T (p.Ile602=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
9 | g.127815989G>C | CA374971983 | ENG | c.1260C>G (p.Ile420Met) c.1806C>G (p.Ile602Met) |