Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
7 | g.87544882G>A | CA4328153 | ABCB1 | c.2005C>T (p.Arg669Cys) c.1813C>T (p.Arg605Cys) c.2215C>T (p.Arg739Cys) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
7 | g.87544882G>C | CA368058865 | ABCB1 | c.2005C>G (p.Arg669Gly) c.1813C>G (p.Arg605Gly) c.2215C>G (p.Arg739Gly) | COSMIC |
7 | g.87544882G= | CA1723646480 | ABCB1 | c.2005C= (p.Arg669=) c.1813C= (p.Arg605=) c.2215C= (p.Arg739=) | |
7 | g.87544882G>T | CA368058866 | ABCB1 | c.2005C>A (p.Arg669Ser) c.1813C>A (p.Arg605Ser) c.2215C>A (p.Arg739Ser) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
7 | g.87544883A= | CA1723646485 | ABCB1 | c.2004T= (p.Thr668=) c.1812T= (p.Thr604=) c.2214T= (p.Thr738=) | |
7 | g.87544883A>C | CA4328154 | ABCB1 | c.2004T>G (p.Thr668=) c.1812T>G (p.Thr604=) c.2214T>G (p.Thr738=) | dbSNP ExAC gnomAD v2 |
7 | g.87544883A>G | CA456358338 | ABCB1 | c.2004T>C (p.Thr668=) c.1812T>C (p.Thr604=) c.2214T>C (p.Thr738=) | |
7 | g.87544883A>T | CA456358340 | ABCB1 | c.2004T>A (p.Thr668=) c.1812T>A (p.Thr604=) c.2214T>A (p.Thr738=) | |
7 | g.87544884G>A | CA368058867 | ABCB1 | c.2003C>T (p.Thr668Ile) c.1811C>T (p.Thr604Ile) c.2213C>T (p.Thr738Ile) | |
7 | g.87544884G>C | CA368058868 | ABCB1 | c.2003C>G (p.Thr668Ser) c.1811C>G (p.Thr604Ser) c.2213C>G (p.Thr738Ser) | |
7 | g.87544884G>T | CA368058869 | ABCB1 | c.2003C>A (p.Thr668Asn) c.1811C>A (p.Thr604Asn) c.2213C>A (p.Thr738Asn) | |
7 | g.87544885T>A | CA368058870 | ABCB1 | c.2002A>T (p.Thr668Ser) c.1810A>T (p.Thr604Ser) c.2212A>T (p.Thr738Ser) | |
7 | g.87544885T>C | CA4328155 | ABCB1 | c.2002A>G (p.Thr668Ala) c.1810A>G (p.Thr604Ala) c.2212A>G (p.Thr738Ala) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
7 | g.87544885T>G | CA368058871 | ABCB1 | c.2002A>C (p.Thr668Pro) c.1810A>C (p.Thr604Pro) c.2212A>C (p.Thr738Pro) | |
7 | g.87544885T= | CA1723646488 | ABCB1 | c.2002A= (p.Thr668=) c.1810A= (p.Thr604=) c.2212A= (p.Thr738=) | |
7 | g.87544886T>A | CA456358345 | ABCB1 | c.2001A>T (p.Ser667=) c.1809A>T (p.Ser603=) c.2211A>T (p.Ser737=) | |
7 | g.87544886T>C | CA456358346 | ABCB1 | c.2001A>G (p.Ser667=) c.1809A>G (p.Ser603=) c.2211A>G (p.Ser737=) | dbSNP gnomAD v3 gnomAD v4 |
7 | g.87544886T>G | CA456358347 | ABCB1 | c.2001A>C (p.Ser667=) c.1809A>C (p.Ser603=) c.2211A>C (p.Ser737=) | |
7 | g.87544887G>A | CA368058874 | ABCB1 | c.2000C>T (p.Ser667Leu) c.1808C>T (p.Ser603Leu) c.2210C>T (p.Ser737Leu) | |
7 | g.87544887G>C | CA368058873 | ABCB1 | c.2000C>G (p.Ser667Ter) c.1808C>G (p.Ser603Ter) c.2210C>G (p.Ser737Ter) | |
7 | g.87544887G>T | CA368058872 | ABCB1 | c.2000C>A (p.Ser667Ter) c.1808C>A (p.Ser603Ter) c.2210C>A (p.Ser737Ter) | |
7 | g.87544888A= | CA1723646492 | ABCB1 | c.1999T= (p.Ser667=) c.1807T= (p.Ser603=) c.2209T= (p.Ser737=) | |
7 | g.87544888A>C | CA368058875 | ABCB1 | c.1999T>G (p.Ser667Ala) c.1807T>G (p.Ser603Ala) c.2209T>G (p.Ser737Ala) | |
7 | g.87544888A>G | CA368058877 | ABCB1 | c.1999T>C (p.Ser667Pro) c.1807T>C (p.Ser603Pro) c.2209T>C (p.Ser737Pro) | dbSNP gnomAD v4 |
7 | g.87544888A>T | CA368058876 | ABCB1 | c.1999T>A (p.Ser667Thr) c.1807T>A (p.Ser603Thr) c.2209T>A (p.Ser737Thr) | COSMIC |
7 | g.87544889T>A | CA368058878 | ABCB1 | c.1998A>T (p.Arg666Ser) c.1806A>T (p.Arg602Ser) c.2208A>T (p.Arg736Ser) | |
7 | g.87544889T>C | CA456358349 | ABCB1 | c.1998A>G (p.Arg666=) c.1806A>G (p.Arg602=) c.2208A>G (p.Arg736=) | |
7 | g.87544889T>G | CA368058880 | ABCB1 | c.1998A>C (p.Arg666Ser) c.1806A>C (p.Arg602Ser) c.2208A>C (p.Arg736Ser) | |
7 | g.87544890C>A | CA4328156 | ABCB1 | c.1997G>T (p.Arg666Ile) c.1805G>T (p.Arg602Ile) c.2207G>T (p.Arg736Ile) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
7 | g.87544890C= | CA1723646499 | ABCB1 | c.1997G= (p.Arg666=) c.1805G= (p.Arg602=) c.2207G= (p.Arg736=) | |
7 | g.87544890C>G | CA368058887 | ABCB1 | c.1997G>C (p.Arg666Thr) c.1805G>C (p.Arg602Thr) c.2207G>C (p.Arg736Thr) | dbSNP gnomAD v4 |
7 | g.87544890C>T | CA368058885 | ABCB1 | c.1997G>A (p.Arg666Lys) c.1805G>A (p.Arg602Lys) c.2207G>A (p.Arg736Lys) | ClinVar dbSNP |
7 | g.87544891T>A | CA368058890 | ABCB1 | c.1996A>T (p.Arg666Ter) c.1804A>T (p.Arg602Ter) c.2206A>T (p.Arg736Ter) | |
7 | g.87544891T>C | CA368058892 | ABCB1 | c.1996A>G (p.Arg666Gly) c.1804A>G (p.Arg602Gly) c.2206A>G (p.Arg736Gly) | |
7 | g.87544891T>G | CA456358353 | ABCB1 | c.1996A>C (p.Arg666=) c.1804A>C (p.Arg602=) c.2206A>C (p.Arg736=) | |
7 | g.87544892T>A | CA368058895 | ABCB1 | c.1995A>T (p.Lys665Asn) c.1803A>T (p.Lys601Asn) c.2205A>T (p.Lys735Asn) | |
7 | g.87544892T>C | CA456358359 | ABCB1 | c.1995A>G (p.Lys665=) c.1803A>G (p.Lys601=) c.2205A>G (p.Lys735=) | |
7 | g.87544892T>G | CA368058897 | ABCB1 | c.1995A>C (p.Lys665Asn) c.1803A>C (p.Lys601Asn) c.2205A>C (p.Lys735Asn) | |
7 | g.87544893T>A | CA368058900 | ABCB1 | c.1994A>T (p.Lys665Ile) c.1802A>T (p.Lys601Ile) c.2204A>T (p.Lys735Ile) | |
7 | g.87544893T>C | CA368058902 | ABCB1 | c.1994A>G (p.Lys665Arg) c.1802A>G (p.Lys601Arg) c.2204A>G (p.Lys735Arg) | dbSNP COSMIC |
7 | g.87544893T>G | CA368058905 | ABCB1 | c.1994A>C (p.Lys665Thr) c.1802A>C (p.Lys601Thr) c.2204A>C (p.Lys735Thr) | gnomAD v4 |
7 | g.87544893T= | CA1723646502 | ABCB1 | c.1994A= (p.Lys665=) c.1802A= (p.Lys601=) c.2204A= (p.Lys735=) | |
7 | g.87544894T>A | CA368058907 | ABCB1 | c.1993A>T (p.Lys665Ter) c.1801A>T (p.Lys601Ter) c.2203A>T (p.Lys735Ter) | |
7 | g.87544894T>C | CA368058909 | ABCB1 | c.1993A>G (p.Lys665Glu) c.1801A>G (p.Lys601Glu) c.2203A>G (p.Lys735Glu) | |
7 | g.87544894T>G | CA4328157 | ABCB1 | c.1993A>C (p.Lys665Gln) c.1801A>C (p.Lys601Gln) c.2203A>C (p.Lys735Gln) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
7 | g.87544894T= | CA1723646506 | ABCB1 | c.1993A= (p.Lys665=) c.1801A= (p.Lys601=) c.2203A= (p.Lys735=) | |
7 | g.87544895T>A | CA368058913 | ABCB1 | c.1992A>T (p.Arg664Ser) c.1800A>T (p.Arg600Ser) c.2202A>T (p.Arg734Ser) | |
7 | g.87544895T>C | CA456358363 | ABCB1 | c.1992A>G (p.Arg664=) c.1800A>G (p.Arg600=) c.2202A>G (p.Arg734=) | gnomAD v4 |
7 | g.87544895T>G | CA368058915 | ABCB1 | c.1992A>C (p.Arg664Ser) c.1800A>C (p.Arg600Ser) c.2202A>C (p.Arg734Ser) | |
7 | g.87544896C>A | CA368058917 | ABCB1 | c.1991G>T (p.Arg664Ile) c.1799G>T (p.Arg600Ile) c.2201G>T (p.Arg734Ile) | COSMIC |