Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
9 | g.130872961G>A | CA16609341 | ABL1 | c.1066G>A (p.Ala356Thr) c.1009G>A (p.Ala337Thr) | ClinVar dbSNP |
9 | g.130872961G>C | CA375249557 | ABL1 | c.1066G>C (p.Ala356Pro) c.1009G>C (p.Ala337Pro) | |
9 | g.130872961G= | CA1881476100 | ABL1 | c.1066G= (p.Ala356=) c.1009G= (p.Ala337=) | |
9 | g.130872961G>T | CA375249558 | ABL1 | c.1066G>T (p.Ala356Ser) c.1009G>T (p.Ala337Ser) | |
9 | g.130872962C>A | CA375249559 | ABL1 | c.1067C>A (p.Ala356Asp) c.1010C>A (p.Ala337Asp) | |
9 | g.130872962C>G | CA375249560 | ABL1 | c.1067C>G (p.Ala356Gly) c.1010C>G (p.Ala337Gly) | |
9 | g.130872962C>T | CA375249561 | ABL1 | c.1067C>T (p.Ala356Val) c.1010C>T (p.Ala337Val) | |
9 | g.130872963dup | CA200645534 | ABL1 | c.1068dup (p.Val357ArgfsTer?) c.1011dup (p.Val338ArgfsTer?) | dbSNP |
9 | g.130872963C>A | CA467395143 | ABL1 | c.1068C>A (p.Ala356=) c.1011C>A (p.Ala337=) | |
9 | g.130872963C= | CA1881476108 | ABL1 | c.1068C= (p.Ala356=) c.1011C= (p.Ala337=) | |
9 | g.130872963C>G | CA467395145 | ABL1 | c.1068C>G (p.Ala356=) c.1011C>G (p.Ala337=) | dbSNP |
9 | g.130872963C>T | CA5285363 | ABL1 | c.1068C>T (p.Ala356=) c.1011C>T (p.Ala337=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC COSMIC COSMIC |
9 | g.130872964G>A | CA375249562 | ABL1 | c.1069G>A (p.Val357Met) c.1012G>A (p.Val338Met) | ClinVar dbSNP |
9 | g.130872964G>C | CA375249563 | ABL1 | c.1069G>C (p.Val357Leu) c.1012G>C (p.Val338Leu) | |
9 | g.130872964G>T | CA375249564 | ABL1 | c.1069G>T (p.Val357Leu) c.1012G>T (p.Val338Leu) | |
9 | g.130872965T>A | CA375249565 | ABL1 | c.1070T>A (p.Val357Glu) c.1013T>A (p.Val338Glu) | |
9 | g.130872965T>C | CA375249566 | ABL1 | c.1070T>C (p.Val357Ala) c.1013T>C (p.Val338Ala) | |
9 | g.130872965T>G | CA375249567 | ABL1 | c.1070T>G (p.Val357Gly) c.1013T>G (p.Val338Gly) | gnomAD v4 |
9 | g.130872966G>A | CA467395146 | ABL1 | c.1071G>A (p.Val357=) c.1014G>A (p.Val338=) | |
9 | g.130872966G>C | CA467395147 | ABL1 | c.1071G>C (p.Val357=) c.1014G>C (p.Val338=) | |
9 | g.130872966G>T | CA467395148 | ABL1 | c.1071G>T (p.Val357=) c.1014G>T (p.Val338=) | |
9 | g.130872967G>A | CA375249570 | ABL1 | c.1072G>A (p.Val358Met) c.1015G>A (p.Val339Met) | dbSNP |
9 | g.130872967G>C | CA375249569 | ABL1 | c.1072G>C (p.Val358Leu) c.1015G>C (p.Val339Leu) | |
9 | g.130872967G>T | CA375249568 | ABL1 | c.1072G>T (p.Val358Leu) c.1015G>T (p.Val339Leu) | |
9 | g.130872968T>A | CA375249571 | ABL1 | c.1073T>A (p.Val358Glu) c.1016T>A (p.Val339Glu) | |
9 | g.130872968T>C | CA375249572 | ABL1 | c.1073T>C (p.Val358Ala) c.1016T>C (p.Val339Ala) | |
9 | g.130872968T>G | CA375249573 | ABL1 | c.1073T>G (p.Val358Gly) c.1016T>G (p.Val339Gly) | |
9 | g.130872969G>A | CA467395153 | ABL1 | c.1074G>A (p.Val358=) c.1017G>A (p.Val339=) | |
9 | g.130872969G>C | CA467395154 | ABL1 | c.1074G>C (p.Val358=) c.1017G>C (p.Val339=) | |
9 | g.130872969G>T | CA467395152 | ABL1 | c.1074G>T (p.Val358=) c.1017G>T (p.Val339=) | |
9 | g.130872970C>A | CA375249574 | ABL1 | c.1075C>A (p.Leu359Met) c.1018C>A (p.Leu340Met) | |
9 | g.130872970C>G | CA375249575 | ABL1 | c.1075C>G (p.Leu359Val) c.1018C>G (p.Leu340Val) | |
9 | g.130872970C>T | CA467395156 | ABL1 | c.1075C>T (p.Leu359=) c.1018C>T (p.Leu340=) | |
9 | g.130872971T>A | CA375249576 | ABL1 | c.1076T>A (p.Leu359Gln) c.1019T>A (p.Leu340Gln) | |
9 | g.130872971T>C | CA375249577 | ABL1 | c.1076T>C (p.Leu359Pro) c.1019T>C (p.Leu340Pro) | |
9 | g.130872971T>G | CA375249578 | ABL1 | c.1076T>G (p.Leu359Arg) c.1019T>G (p.Leu340Arg) | |
9 | g.130872972G>A | CA467395157 | ABL1 | c.1077G>A (p.Leu359=) c.1020G>A (p.Leu340=) | dbSNP gnomAD v4 |
9 | g.130872972G>C | CA467395158 | ABL1 | c.1077G>C (p.Leu359=) c.1020G>C (p.Leu340=) | dbSNP |
9 | g.130872972G= | CA1881476112 | ABL1 | c.1077G= (p.Leu359=) c.1020G= (p.Leu340=) | |
9 | g.130872972G>T | CA467395159 | ABL1 | c.1077G>T (p.Leu359=) c.1020G>T (p.Leu340=) | |
9 | g.130872973C>A | CA375249579 | ABL1 | c.1078C>A (p.Leu360Met) c.1021C>A (p.Leu341Met) | |
9 | g.130872973C>G | CA375249580 | ABL1 | c.1078C>G (p.Leu360Val) c.1021C>G (p.Leu341Val) | |
9 | g.130872973C>T | CA467395160 | ABL1 | c.1078C>T (p.Leu360=) c.1021C>T (p.Leu341=) | gnomAD v4 |
9 | g.130872974T>A | CA375249582 | ABL1 | c.1079T>A (p.Leu360Gln) c.1022T>A (p.Leu341Gln) | |
9 | g.130872974T>C | CA375249583 | ABL1 | c.1079T>C (p.Leu360Pro) c.1022T>C (p.Leu341Pro) | |
9 | g.130872974T>G | CA375249584 | ABL1 | c.1079T>G (p.Leu360Arg) c.1022T>G (p.Leu341Arg) | |
9 | g.130872975G>A | CA467395162 | ABL1 | c.1080G>A (p.Leu360=) c.1023G>A (p.Leu341=) | dbSNP |
9 | g.130872975G>C | CA5285364 | ABL1 | c.1080G>C (p.Leu360=) c.1023G>C (p.Leu341=) | dbSNP ExAC gnomAD v2 gnomAD v4 |
9 | g.130872975G= | CA1881476120 | ABL1 | c.1080G= (p.Leu360=) c.1023G= (p.Leu341=) | |
9 | g.130872975G>T | CA467395163 | ABL1 | c.1080G>T (p.Leu360=) c.1023G>T (p.Leu341=) |