Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
15 | g.74754997T>A | CA393170349 | CYP1A2 | c.1460T>A (p.Val487Glu) | |
15 | g.74754997T>C | CA393170352 | CYP1A2 | c.1460T>C (p.Val487Ala) | |
15 | g.74754997T>G | CA393170355 | CYP1A2 | c.1460T>G (p.Val487Gly) | |
15 | g.74754998G>A | CA491489791 | CYP1A2 | c.1461G>A (p.Val487=) | |
15 | g.74754998G>C | CA491489792 | CYP1A2 | c.1461G>C (p.Val487=) | |
15 | g.74754998G= | CA2187827139 | CYP1A2 | c.1461G= (p.Val487=) | |
15 | g.74754998G>T | CA491489793 | CYP1A2 | c.1461G>T (p.Val487=) | dbSNP gnomAD v3 gnomAD v4 |
15 | g.74754999A= | CA2187827140 | CYP1A2 | c.1462A= (p.Lys488=) | |
15 | g.74754999A>C | CA393170357 | CYP1A2 | c.1462A>C (p.Lys488Gln) | |
15 | g.74754999A>G | CA393170360 | CYP1A2 | c.1462A>G (p.Lys488Glu) | dbSNP gnomAD v2 gnomAD v4 |
15 | g.74754999A>T | CA393170359 | CYP1A2 | c.1462A>T (p.Lys488Ter) | |
15 | g.74755000A>C | CA393170362 | CYP1A2 | c.1463A>C (p.Lys488Thr) | |
15 | g.74755000A>G | CA393170365 | CYP1A2 | c.1463A>G (p.Lys488Arg) | |
15 | g.74755000A>T | CA393170370 | CYP1A2 | c.1463A>T (p.Lys488Ile) | COSMIC |
15 | g.74755001A>C | CA393170372 | CYP1A2 | c.1464A>C (p.Lys488Asn) | |
15 | g.74755001A>G | CA491489794 | CYP1A2 | c.1464A>G (p.Lys488=) | |
15 | g.74755001A>T | CA393170374 | CYP1A2 | c.1464A>T (p.Lys488Asn) | |
15 | g.74755002G>A | CA272816157 | CYP1A2 | c.1465G>A (p.Val489Ile) | dbSNP |
15 | g.74755002G>C | CA393170379 | CYP1A2 | c.1465G>C (p.Val489Leu) | |
15 | g.74755002G= | CA2187827141 | CYP1A2 | c.1465G= (p.Val489=) | |
15 | g.74755002G>T | CA393170377 | CYP1A2 | c.1465G>T (p.Val489Phe) | |
15 | g.74755003T>A | CA393170382 | CYP1A2 | c.1466T>A (p.Val489Asp) | |
15 | g.74755003T>C | CA393170384 | CYP1A2 | c.1466T>C (p.Val489Ala) | |
15 | g.74755003T>G | CA393170388 | CYP1A2 | c.1466T>G (p.Val489Gly) | |
15 | g.74755004C>A | CA491489795 | CYP1A2 | c.1467C>A (p.Val489=) | |
15 | g.74755004C= | CA2187827142 | CYP1A2 | c.1467C= (p.Val489=) | |
15 | g.74755004C>G | CA491489796 | CYP1A2 | c.1467C>G (p.Val489=) | |
15 | g.74755004C>T | CA491489797 | CYP1A2 | c.1467C>T (p.Val489=) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
15 | g.74755005G>A | CA7660122 | CYP1A2 | c.1468G>A (p.Asp490Asn) | dbSNP ExAC gnomAD v2 gnomAD v4 COSMIC |
15 | g.74755005G>C | CA393170396 | CYP1A2 | c.1468G>C (p.Asp490His) | |
15 | g.74755005G= | CA2187827143 | CYP1A2 | c.1468G= (p.Asp490=) | |
15 | g.74755005G>T | CA393170398 | CYP1A2 | c.1468G>T (p.Asp490Tyr) | |
15 | g.74755006A>C | CA393170401 | CYP1A2 | c.1469A>C (p.Asp490Ala) | |
15 | g.74755006A>G | CA393170402 | CYP1A2 | c.1469A>G (p.Asp490Gly) | COSMIC |
15 | g.74755006A>T | CA393170403 | CYP1A2 | c.1469A>T (p.Asp490Val) | gnomAD v4 |
15 | g.74755007C>A | CA393170404 | CYP1A2 | c.1470C>A (p.Asp490Glu) | |
15 | g.74755007C= | CA2187827145 | CYP1A2 | c.1470C= (p.Asp490=) | |
15 | g.74755007C>G | CA393170405 | CYP1A2 | c.1470C>G (p.Asp490Glu) | |
15 | g.74755007C>T | CA491489798 | CYP1A2 | c.1470C>T (p.Asp490=) | |
15 | g.74755007_74755025delinsCCTGACCCCCATCTACGGG | CA2187827144 | CYP1A2 | c.1470_1488delinsCCTGACCCCCATCTACGGG (p.Asp490=) | |
15 | g.74755008C>A | CA393170407 | CYP1A2 | c.1471C>A (p.Leu491Met) | dbSNP gnomAD v4 |
15 | g.74755008C= | CA2187827147 | CYP1A2 | c.1471C= (p.Leu491=) | |
15 | g.74755008C>G | CA393170409 | CYP1A2 | c.1471C>G (p.Leu491Val) | dbSNP gnomAD v3 gnomAD v4 |
15 | g.74755008C>T | CA491489799 | CYP1A2 | c.1471C>T (p.Leu491=) | |
15 | g.74755009_74755012dup | CA2187827146 | CYP1A2 | c.1472_1475dup (p.Pro493AspfsTer14) | dbSNP gnomAD v4 |
15 | g.74755014_74755031del | CA715670998 | CYP1A2 | c.1477_1494del (p.Pro493_Thr498del) | dbSNP gnomAD v4 |
15 | g.74755009T>A | CA393170422 | CYP1A2 | c.1472T>A (p.Leu491Gln) | |
15 | g.74755009T>C | CA393170424 | CYP1A2 | c.1472T>C (p.Leu491Pro) | |
15 | g.74755009T>G | CA393170411 | CYP1A2 | c.1472T>G (p.Leu491Arg) | |
15 | g.74755010G>A | CA491489800 | CYP1A2 | c.1473G>A (p.Leu491=) |