Chr Mutation (hg38) CAid Gene Transcript Linkouts
12g.20892663T>CCA603641812SLCO1B3c.1683-5773T>C (p.=)
c.1599-5773T>C (p.=)
c.359+34092T>C (p.=)
n.1155-5773T>C (p.=)
gnomAD
12g.20892663T>GCA233500879SLCO1B3c.1683-5773T>G (p.=)
c.1599-5773T>G (p.=)
c.359+34092T>G (p.=)
n.1155-5773T>G (p.=)
dbSNP
12g.20892664A>GCA233500896SLCO1B3c.1683-5772A>G (p.=)
c.1599-5772A>G (p.=)
c.359+34093A>G (p.=)
n.1155-5772A>G (p.=)
dbSNP
12g.20892670G>ACA233500897SLCO1B3c.1683-5766G>A (p.=)
c.1599-5766G>A (p.=)
c.359+34099G>A (p.=)
n.1155-5766G>A (p.=)
dbSNP
12g.20892677A>GCA686350910SLCO1B3c.1683-5759A>G (p.=)
c.1599-5759A>G (p.=)
c.359+34106A>G (p.=)
n.1155-5759A>G (p.=)
12g.20892682G>TCA233500901SLCO1B3c.1683-5754G>T (p.=)
c.1599-5754G>T (p.=)
c.359+34111G>T (p.=)
n.1155-5754G>T (p.=)
dbSNP gnomAD
12g.20892694_20892711dupCA233500906SLCO1B3c.1683-5742_1683-5725dup (p.=)
c.1599-5742_1599-5725dup (p.=)
c.359+34123_359+34140dup (p.=)
n.1155-5742_1155-5725dup (p.=)
dbSNP
12g.20892690A>GCA603641814SLCO1B3c.1683-5746A>G (p.=)
c.1599-5746A>G (p.=)
c.359+34119A>G (p.=)
n.1155-5746A>G (p.=)
gnomAD
12g.20892690_20892691delCA686350916SLCO1B3c.1683-5746_1683-5745del (p.=)
c.1599-5746_1599-5745del (p.=)
c.359+34119_359+34120del (p.=)
n.1155-5746_1155-5745del (p.=)
dbSNP
12g.20892700delCA945442127SLCO1B3c.1683-5736del (p.=)
c.1599-5736del (p.=)
c.359+34129del (p.=)
n.1155-5736del (p.=)
12g.20892701A>GCA603641816SLCO1B3c.1683-5735A>G (p.=)
c.1599-5735A>G (p.=)
c.359+34130A>G (p.=)
n.1155-5735A>G (p.=)
gnomAD
12g.20892702_20892703insGCA945442134SLCO1B3c.1683-5734_1683-5733insG (p.=)
c.1599-5734_1599-5733insG (p.=)
c.359+34131_359+34132insG (p.=)
n.1155-5734_1155-5733insG (p.=)
12g.20892703_20892704insGAAAGAGGAGGAAGAATCA945442137SLCO1B3c.1683-5733_1683-5732insGAAAGAGGAGGAAGAAT (p.=)
c.1599-5733_1599-5732insGAAAGAGGAGGAAGAAT (p.=)
c.359+34132_359+34133insGAAAGAGGAGGAAGAAT (p.=)
n.1155-5733_1155-5732insGAAAGAGGAGGAAGAAT (p.=)
12g.20892707A>GCA233500909SLCO1B3c.1683-5729A>G (p.=)
c.1599-5729A>G (p.=)
c.359+34136A>G (p.=)
n.1155-5729A>G (p.=)
dbSNP
12g.20892708A>GCA233500918SLCO1B3c.1683-5728A>G (p.=)
c.1599-5728A>G (p.=)
c.359+34137A>G (p.=)
n.1155-5728A>G (p.=)
dbSNP gnomAD
12g.20892708A>TCA233500929SLCO1B3c.1683-5728A>T (p.=)
c.1599-5728A>T (p.=)
c.359+34137A>T (p.=)
n.1155-5728A>T (p.=)
dbSNP
12g.20892708_20892709delCA233500913SLCO1B3c.1683-5728_1683-5727del (p.=)
c.1599-5728_1599-5727del (p.=)
c.359+34137_359+34138del (p.=)
n.1155-5728_1155-5727del (p.=)
dbSNP gnomAD
12g.20892709G>ACA686350927SLCO1B3c.1683-5727G>A (p.=)
c.1599-5727G>A (p.=)
c.359+34138G>A (p.=)
n.1155-5727G>A (p.=)
12g.20892711G>ACA654196493SLCO1B3c.1683-5725G>A (p.=)
c.1599-5725G>A (p.=)
c.359+34140G>A (p.=)
n.1155-5725G>A (p.=)
COSMIC
12g.20892728T>CCA233500934SLCO1B3c.1683-5708T>C (p.=)
c.1599-5708T>C (p.=)
c.359+34157T>C (p.=)
n.1155-5708T>C (p.=)
dbSNP gnomAD
12g.20892732A>CCA233500940SLCO1B3c.1683-5704A>C (p.=)
c.1599-5704A>C (p.=)
c.359+34161A>C (p.=)
n.1155-5704A>C (p.=)
dbSNP
12g.20892733A>CCA603641821SLCO1B3c.1683-5703A>C (p.=)
c.1599-5703A>C (p.=)
c.359+34162A>C (p.=)
n.1155-5703A>C (p.=)
gnomAD
12g.20892733A>GCA686350930SLCO1B3c.1683-5703A>G (p.=)
c.1599-5703A>G (p.=)
c.359+34162A>G (p.=)
n.1155-5703A>G (p.=)
12g.20892734C>GCA478860397SLCO1B3c.1683-5702C>G (p.=)
c.1599-5702C>G (p.=)
c.359+34163C>G (p.=)
n.1155-5702C>G (p.=)
12g.20892734C>TCA603641823SLCO1B3c.1683-5702C>T (p.=)
c.1599-5702C>T (p.=)
c.359+34163C>T (p.=)
n.1155-5702C>T (p.=)
gnomAD
12g.20892740A>GCA686350931SLCO1B3c.1683-5696A>G (p.=)
c.1599-5696A>G (p.=)
c.359+34169A>G (p.=)
n.1155-5696A>G (p.=)
12g.20892745G>ACA686350934SLCO1B3c.1683-5691G>A (p.=)
c.1599-5691G>A (p.=)
c.359+34174G>A (p.=)
n.1155-5691G>A (p.=)
12g.20892756delCA945442149SLCO1B3c.1683-5680del (p.=)
c.1599-5680del (p.=)
c.359+34185del (p.=)
n.1155-5680del (p.=)
12g.20892759C>TCA686350937SLCO1B3c.1683-5677C>T (p.=)
c.1599-5677C>T (p.=)
c.359+34188C>T (p.=)
n.1155-5677C>T (p.=)
12g.20892760A>GCA13581915SLCO1B3c.1683-5676A>G (p.=)
c.1599-5676A>G (p.=)
c.359+34189A>G (p.=)
n.1155-5676A>G (p.=)
dbSNP gnomAD

Number of alleles fetched