Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
4 | g.88131171del | CA2671372361 | ABCG2 | c.421del (p.Gln141SerfsTer12) | gnomAD v4 |
4 | g.88131171G>A | CA357630432 | ABCG2 | c.421C>T (p.Gln141Ter) | dbSNP |
4 | g.88131171G>C | CA357630433 | ABCG2 | c.421C>G (p.Gln141Glu) | dbSNP gnomAD v3 gnomAD v4 |
4 | g.88131171G= | CA1474616670 | ABCG2 | c.421C= (p.Gln141=) | |
4 | g.88131171G>T | CA129179 | ABCG2 | c.421C>A (p.Gln141Lys) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
4 | g.88131172T>A | CA357630434 | ABCG2 | c.420A>T (p.Leu140Phe) | dbSNP gnomAD v4 |
4 | g.88131172T>C | CA440271013 | ABCG2 | c.420A>G (p.Leu140=) | |
4 | g.88131172T>G | CA357630435 | ABCG2 | c.420A>C (p.Leu140Phe) | |
4 | g.88131172T= | CA1474616672 | ABCG2 | c.420A= (p.Leu140=) | |
4 | g.88131172dup | CA552870978 | ABCG2 | c.420dup (p.Gln141ThrfsTer16) | dbSNP gnomAD v2 gnomAD v4 |
4 | g.88131172_88131173delinsTA | CA1474616671 | ABCG2 | c.419_420delinsTA (p.Leu140=) | |
4 | g.88131172_88131174delinsTAA | CA1474616673 | ABCG2 | c.418_420delinsTTA (p.Leu140=) | |
4 | g.88131173A= | CA1474616675 | ABCG2 | c.419T= (p.Leu140=) | |
4 | g.88131173A>C | CA357630436 | ABCG2 | c.419T>G (p.Leu140Ter) | dbSNP |
4 | g.88131173A>G | CA357630437 | ABCG2 | c.419T>C (p.Leu140Ser) | |
4 | g.88131173A>T | CA357630438 | ABCG2 | c.419T>A (p.Leu140Ter) | |
4 | g.88131173_88131174del | CA1474616674 | ABCG2 | c.418_419del (p.Leu140ThrfsTer16) | dbSNP |
4 | g.88131174del | CA658796451 | ABCG2 | c.419del (p.Leu140TyrfsTer13) | ClinVar dbSNP |
4 | g.88131173_88131175del | CA2671372362 | ABCG2 | c.417_419del (p.Asn139_Leu140delinsLys) | gnomAD v4 |
4 | g.88131174A= | CA1474616676 | ABCG2 | c.418T= (p.Leu140=) | |
4 | g.88131174A>C | CA357630439 | ABCG2 | c.418T>G (p.Leu140Val) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 COSMIC COSMIC |
4 | g.88131174A>G | CA440271020 | ABCG2 | c.418T>C (p.Leu140=) | |
4 | g.88131174A>T | CA357630440 | ABCG2 | c.418T>A (p.Leu140Ile) | |
4 | g.88131175G>A | CA440271025 | ABCG2 | c.417C>T (p.Asn139=) | |
4 | g.88131175G>C | CA357630441 | ABCG2 | c.417C>G (p.Asn139Lys) | gnomAD v4 |
4 | g.88131175G>T | CA357630442 | ABCG2 | c.417C>A (p.Asn139Lys) | |
4 | g.88131176T>A | CA357630443 | ABCG2 | c.416A>T (p.Asn139Ile) | |
4 | g.88131176T>C | CA357630444 | ABCG2 | c.416A>G (p.Asn139Ser) | dbSNP gnomAD v4 |
4 | g.88131176T>G | CA357630445 | ABCG2 | c.416A>C (p.Asn139Thr) | |
4 | g.88131176T= | CA1474616677 | ABCG2 | c.416A= (p.Asn139=) | |
4 | g.88131177T>A | CA357630446 | ABCG2 | c.415A>T (p.Asn139Tyr) | |
4 | g.88131177T>C | CA357630448 | ABCG2 | c.415A>G (p.Asn139Asp) | gnomAD v4 |
4 | g.88131177T>G | CA357630447 | ABCG2 | c.415A>C (p.Asn139His) | |
4 | g.88131178_88131183del | CA2671372363 | ABCG2 | c.410_415del (p.Arg137_Glu138del) | gnomAD v4 |
4 | g.88131178T>A | CA357630449 | ABCG2 | c.414A>T (p.Glu138Asp) | |
4 | g.88131178T>C | CA440271054 | ABCG2 | c.414A>G (p.Glu138=) | |
4 | g.88131178T>G | CA357630450 | ABCG2 | c.414A>C (p.Glu138Asp) | |
4 | g.88131179T>A | CA357630451 | ABCG2 | c.413A>T (p.Glu138Val) | |
4 | g.88131179T>C | CA357630452 | ABCG2 | c.413A>G (p.Glu138Gly) | |
4 | g.88131179T>G | CA357630453 | ABCG2 | c.413A>C (p.Glu138Ala) | |
4 | g.88131180C>A | CA357630454 | ABCG2 | c.412G>T (p.Glu138Ter) | COSMIC COSMIC |
4 | g.88131180C= | CA1474616678 | ABCG2 | c.412G= (p.Glu138=) | |
4 | g.88131180C>G | CA357630455 | ABCG2 | c.412G>C (p.Glu138Gln) | COSMIC COSMIC |
4 | g.88131180C>T | CA100893428 | ABCG2 | c.412G>A (p.Glu138Lys) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
4 | g.88131181T>A | CA357630456 | ABCG2 | c.411A>T (p.Arg137Ser) | |
4 | g.88131181T>C | CA440271069 | ABCG2 | c.411A>G (p.Arg137=) | |
4 | g.88131181T>G | CA357630457 | ABCG2 | c.411A>C (p.Arg137Ser) | |
4 | g.88131182C>A | CA357630458 | ABCG2 | c.410G>T (p.Arg137Ile) | |
4 | g.88131182C= | CA1474616679 | ABCG2 | c.410G= (p.Arg137=) | |
4 | g.88131182C>G | CA3004924 | ABCG2 | c.410G>C (p.Arg137Thr) | dbSNP ExAC gnomAD v2 gnomAD v4 |