Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
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=) | |
15 | g.74755010G>C | CA491489801 | CYP1A2 | c.1473G>C (p.Leu491=) | |
15 | g.74755010G= | CA2187827148 | CYP1A2 | c.1473G= (p.Leu491=) | |
15 | g.74755010G>T | CA7660123 | CYP1A2 | c.1473G>T (p.Leu491=) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
15 | g.74755011A= | CA2187827149 | CYP1A2 | c.1474A= (p.Thr492=) | |
15 | g.74755011A>C | CA393170429 | CYP1A2 | c.1474A>C (p.Thr492Pro) | dbSNP gnomAD v2 gnomAD v4 |
15 | g.74755011A>G | CA393170437 | CYP1A2 | c.1474A>G (p.Thr492Ala) | |
15 | g.74755011A>T | CA393170431 | CYP1A2 | c.1474A>T (p.Thr492Ser) | |
15 | g.74755011_74755012delinsAC | CA2187827150 | CYP1A2 | c.1474_1475delinsAC (p.Thr492=) | |
15 | g.74755012C>A | CA393170440 | CYP1A2 | c.1475C>A (p.Thr492Asn) | gnomAD v4 |
15 | g.74755012C>G | CA393170445 | CYP1A2 | c.1475C>G (p.Thr492Ser) | |
15 | g.74755012C>T | CA393170442 | CYP1A2 | c.1475C>T (p.Thr492Ile) | gnomAD v4 |
15 | g.74755016del | CA715671010 | CYP1A2 | c.1479del (p.Ile494SerfsTer4) | dbSNP gnomAD v3 gnomAD v4 |
15 | g.74755013C>A | CA491489802 | CYP1A2 | c.1476C>A (p.Thr492=) | gnomAD v4 |
15 | g.74755013C= | CA2187827151 | CYP1A2 | c.1476C= (p.Thr492=) | |
15 | g.74755013C>G | CA491489803 | CYP1A2 | c.1476C>G (p.Thr492=) | |
15 | g.74755013C>T | CA491489804 | CYP1A2 | c.1476C>T (p.Thr492=) | dbSNP gnomAD v2 gnomAD v4 |
15 | g.74755014C>A | CA393170451 | CYP1A2 | c.1477C>A (p.Pro493Thr) | |
15 | g.74755014C>G | CA393170457 | CYP1A2 | c.1477C>G (p.Pro493Ala) | |
15 | g.74755014C>T | CA393170454 | CYP1A2 | c.1477C>T (p.Pro493Ser) | |
15 | g.74755015C>A | CA393170463 | CYP1A2 | c.1478C>A (p.Pro493His) | |
15 | g.74755015C>G | CA393170468 | CYP1A2 | c.1478C>G (p.Pro493Arg) | |
15 | g.74755015C>T | CA393170467 | CYP1A2 | c.1478C>T (p.Pro493Leu) | gnomAD v4 |
15 | g.74755016C>A | CA491489805 | CYP1A2 | c.1479C>A (p.Pro493=) | |
15 | g.74755016C>G | CA491489806 | CYP1A2 | c.1479C>G (p.Pro493=) |