| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 12 | g.20892760A>G | CA13581915 | SLCO1B3 | c.1683-5676A>G (p.=) c.1599-5676A>G (p.=) c.359+34189A>G (p.=) n.1155-5676A>G (p.=) | dbSNP gnomAD |
| 12 | g.20892767C>A | CA233500963 | SLCO1B3 | c.1683-5669C>A (p.=) c.1599-5669C>A (p.=) c.359+34196C>A (p.=) n.1155-5669C>A (p.=) | dbSNP gnomAD |
| 12 | g.20892768A>C | CA686350944 | SLCO1B3 | c.1683-5668A>C (p.=) c.1599-5668A>C (p.=) c.359+34197A>C (p.=) n.1155-5668A>C (p.=) | |
| 12 | g.20892768A>G | CA233500974 | SLCO1B3 | c.1683-5668A>G (p.=) c.1599-5668A>G (p.=) c.359+34197A>G (p.=) n.1155-5668A>G (p.=) | dbSNP |
| 12 | g.20892775A>G | CA233500989 | SLCO1B3 | c.1683-5661A>G (p.=) c.1599-5661A>G (p.=) c.359+34204A>G (p.=) n.1155-5661A>G (p.=) | dbSNP |
| 12 | g.20892781T>C | CA233500997 | SLCO1B3 | c.1683-5655T>C (p.=) c.1599-5655T>C (p.=) c.359+34210T>C (p.=) n.1155-5655T>C (p.=) | dbSNP gnomAD |
| 12 | g.20892781T>G | CA233501003 | SLCO1B3 | c.1683-5655T>G (p.=) c.1599-5655T>G (p.=) c.359+34210T>G (p.=) n.1155-5655T>G (p.=) | dbSNP gnomAD |
| 12 | g.20892787A>C | CA233501004 | SLCO1B3 | c.1683-5649A>C (p.=) c.1599-5649A>C (p.=) c.359+34216A>C (p.=) n.1155-5649A>C (p.=) | dbSNP |
| 12 | g.20892796C>T | CA603641829 | SLCO1B3 | c.1683-5640C>T (p.=) c.1599-5640C>T (p.=) c.359+34225C>T (p.=) n.1155-5640C>T (p.=) | gnomAD |
| 12 | g.20892797G>A | CA603641831 | SLCO1B3 | c.1683-5639G>A (p.=) c.1599-5639G>A (p.=) c.359+34226G>A (p.=) n.1155-5639G>A (p.=) | gnomAD |
| 12 | g.20892799del | CA233501005 | SLCO1B3 | c.1683-5637del (p.=) c.1599-5637del (p.=) c.359+34228del (p.=) n.1155-5637del (p.=) | dbSNP |
| 12 | g.20892800T>A | CA686350951 | SLCO1B3 | c.1683-5636T>A (p.=) c.1599-5636T>A (p.=) c.359+34229T>A (p.=) n.1155-5636T>A (p.=) | |
| 12 | g.20892802C>A | CA945442161 | SLCO1B3 | c.1683-5634C>A (p.=) c.1599-5634C>A (p.=) c.359+34231C>A (p.=) n.1155-5634C>A (p.=) | |
| 12 | g.20892802C>T | CA686350954 | SLCO1B3 | c.1683-5634C>T (p.=) c.1599-5634C>T (p.=) c.359+34231C>T (p.=) n.1155-5634C>T (p.=) | |
| 12 | g.20892814C>T | CA686350956 | SLCO1B3 | c.1683-5622C>T (p.=) c.1599-5622C>T (p.=) c.359+34243C>T (p.=) n.1155-5622C>T (p.=) | |
| 12 | g.20892819A>G | CA233501007 | SLCO1B3 | c.1683-5617A>G (p.=) c.1599-5617A>G (p.=) c.359+34248A>G (p.=) n.1155-5617A>G (p.=) | dbSNP |
| 12 | g.20892819_20892825dup | CA233501006 | SLCO1B3 | c.1683-5617_1683-5611dup (p.=) c.1599-5617_1599-5611dup (p.=) c.359+34248_359+34254dup (p.=) n.1155-5617_1155-5611dup (p.=) | dbSNP gnomAD |
| 12 | g.20892824T>A | CA686350965 | SLCO1B3 | c.1683-5612T>A (p.=) c.1599-5612T>A (p.=) c.359+34253T>A (p.=) n.1155-5612T>A (p.=) | |
| 12 | g.20892824_20892825del | CA233501008 | SLCO1B3 | c.1683-5612_1683-5611del (p.=) c.1599-5612_1599-5611del (p.=) c.359+34253_359+34254del (p.=) n.1155-5612_1155-5611del (p.=) | dbSNP gnomAD |
| 12 | g.20892826T>C | CA686350977 | SLCO1B3 | c.1683-5610T>C (p.=) c.1599-5610T>C (p.=) c.359+34255T>C (p.=) n.1155-5610T>C (p.=) | |
| 12 | g.20892829T>C | CA603641834 | SLCO1B3 | c.1683-5607T>C (p.=) c.1599-5607T>C (p.=) c.359+34258T>C (p.=) n.1155-5607T>C (p.=) | gnomAD |
| 12 | g.20892829T>G | CA233501009 | SLCO1B3 | c.1683-5607T>G (p.=) c.1599-5607T>G (p.=) c.359+34258T>G (p.=) n.1155-5607T>G (p.=) | dbSNP |
| 12 | g.20892834A>T | CA603641836 | SLCO1B3 | c.1683-5602A>T (p.=) c.1599-5602A>T (p.=) c.359+34263A>T (p.=) n.1155-5602A>T (p.=) | gnomAD |
| 12 | g.20892840A>G | CA233501011 | SLCO1B3 | c.1683-5596A>G (p.=) c.1599-5596A>G (p.=) c.359+34269A>G (p.=) n.1155-5596A>G (p.=) | dbSNP |
| 12 | g.20892842G>C | CA233501013 | SLCO1B3 | c.1683-5594G>C (p.=) c.1599-5594G>C (p.=) c.359+34271G>C (p.=) n.1155-5594G>C (p.=) | dbSNP gnomAD |
| 12 | g.20892846G>C | CA233501016 | SLCO1B3 | c.1683-5590G>C (p.=) c.1599-5590G>C (p.=) c.359+34275G>C (p.=) n.1155-5590G>C (p.=) | dbSNP |
| 12 | g.20892856A>G | CA233501030 | SLCO1B3 | c.1683-5580A>G (p.=) c.1599-5580A>G (p.=) c.359+34285A>G (p.=) n.1155-5580A>G (p.=) | dbSNP gnomAD |