Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
15 | g.74754828C>A | CA491489606 | CYP1A2 | c.1291C>A (p.Arg431=) | |
15 | g.74754828C= | CA2187827052 | CYP1A2 | c.1291C= (p.Arg431=) | |
15 | g.74754828C>G | CA393169221 | CYP1A2 | c.1291C>G (p.Arg431Gly) | |
15 | g.74754828C>T | CA7660065 | CYP1A2 | c.1291C>T (p.Arg431Trp) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
15 | g.74754829G>A | CA393169228 | CYP1A2 | c.1292G>A (p.Arg431Gln) | dbSNP gnomAD v2 gnomAD v4 |
15 | g.74754829G>C | CA393169229 | CYP1A2 | c.1292G>C (p.Arg431Pro) | dbSNP gnomAD v2 gnomAD v4 |
15 | g.74754829G= | CA2187827053 | CYP1A2 | c.1292G= (p.Arg431=) | |
15 | g.74754829G>T | CA393169231 | CYP1A2 | c.1292G>T (p.Arg431Leu) | dbSNP gnomAD v2 gnomAD v4 |
15 | g.74754830dup | CA7660066 | CYP1A2 | c.1293dup (p.Phe432ValfsTer10) | dbSNP ExAC gnomAD v2 gnomAD v4 |
15 | g.74754830G>A | CA491489614 | CYP1A2 | c.1293G>A (p.Arg431=) | dbSNP gnomAD v4 |
15 | g.74754830G>C | CA7660067 | CYP1A2 | c.1293G>C (p.Arg431=) | dbSNP ExAC gnomAD v2 gnomAD v4 |
15 | g.74754830G= | CA2187827054 | CYP1A2 | c.1293G= (p.Arg431=) | |
15 | g.74754830G>T | CA491489616 | CYP1A2 | c.1293G>T (p.Arg431=) | dbSNP |
15 | g.74754831T>A | CA393169237 | CYP1A2 | c.1294T>A (p.Phe432Ile) | |
15 | g.74754831T>C | CA393169240 | CYP1A2 | c.1294T>C (p.Phe432Leu) | gnomAD v4 |
15 | g.74754831T>G | CA393169238 | CYP1A2 | c.1294T>G (p.Phe432Val) | |
15 | g.74754832T>A | CA393169242 | CYP1A2 | c.1295T>A (p.Phe432Tyr) | |
15 | g.74754832T>C | CA7660068 | CYP1A2 | c.1295T>C (p.Phe432Ser) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
15 | g.74754832T>G | CA393169245 | CYP1A2 | c.1295T>G (p.Phe432Cys) | gnomAD v4 |
15 | g.74754832T= | CA2187827055 | CYP1A2 | c.1295T= (p.Phe432=) | |
15 | g.74754833C>A | CA393169249 | CYP1A2 | c.1296C>A (p.Phe432Leu) | |
15 | g.74754833C= | CA2187827056 | CYP1A2 | c.1296C= (p.Phe432=) | |
15 | g.74754833C>G | CA393169250 | CYP1A2 | c.1296C>G (p.Phe432Leu) | |
15 | g.74754833C>T | CA491489623 | CYP1A2 | c.1296C>T (p.Phe432=) | dbSNP gnomAD v2 gnomAD v4 |
15 | g.74754834dup | CA491489621 | CYP1A2 | c.1297dup (p.Leu433ProfsTer9) | COSMIC |
15 | g.74754834C>A | CA393169253 | CYP1A2 | c.1297C>A (p.Leu433Ile) | |
15 | g.74754834C>G | CA393169256 | CYP1A2 | c.1297C>G (p.Leu433Val) | |
15 | g.74754834C>T | CA393169259 | CYP1A2 | c.1297C>T (p.Leu433Phe) | |
15 | g.74754835T>A | CA393169261 | CYP1A2 | c.1298T>A (p.Leu433His) | |
15 | g.74754835T>C | CA393169263 | CYP1A2 | c.1298T>C (p.Leu433Pro) | |
15 | g.74754835T>G | CA393169265 | CYP1A2 | c.1298T>G (p.Leu433Arg) | |
15 | g.74754836C>A | CA491489627 | CYP1A2 | c.1299C>A (p.Leu433=) | gnomAD v4 |
15 | g.74754836C= | CA2187827057 | CYP1A2 | c.1299C= (p.Leu433=) | |
15 | g.74754836C>G | CA491489628 | CYP1A2 | c.1299C>G (p.Leu433=) | |
15 | g.74754836C>T | CA491489629 | CYP1A2 | c.1299C>T (p.Leu433=) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
15 | g.74754837A= | CA2187827058 | CYP1A2 | c.1300A= (p.Thr434=) | |
15 | g.74754837A>C | CA7660069 | CYP1A2 | c.1300A>C (p.Thr434Pro) | dbSNP ExAC gnomAD v2 |
15 | g.74754837A>G | CA393169272 | CYP1A2 | c.1300A>G (p.Thr434Ala) | COSMIC |
15 | g.74754837A>T | CA393169269 | CYP1A2 | c.1300A>T (p.Thr434Ser) | |
15 | g.74754838C>A | CA393169284 | CYP1A2 | c.1301C>A (p.Thr434Asn) | |
15 | g.74754838C>G | CA393169287 | CYP1A2 | c.1301C>G (p.Thr434Ser) | |
15 | g.74754838C>T | CA393169288 | CYP1A2 | c.1301C>T (p.Thr434Ile) | gnomAD v4 |
15 | g.74754839C>A | CA491489632 | CYP1A2 | c.1302C>A (p.Thr434=) | |
15 | g.74754839C= | CA2187827059 | CYP1A2 | c.1302C= (p.Thr434=) | |
15 | g.74754839C>G | CA491489633 | CYP1A2 | c.1302C>G (p.Thr434=) | gnomAD v4 |
15 | g.74754839C>T | CA7660070 | CYP1A2 | c.1302C>T (p.Thr434=) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
15 | g.74754840G>A | CA393169293 | CYP1A2 | c.1303G>A (p.Ala435Thr) | dbSNP gnomAD v3 gnomAD v4 |
15 | g.74754840G>C | CA393169295 | CYP1A2 | c.1303G>C (p.Ala435Pro) | |
15 | g.74754840G= | CA2187827060 | CYP1A2 | c.1303G= (p.Ala435=) | |
15 | g.74754840G>T | CA393169298 | CYP1A2 | c.1303G>T (p.Ala435Ser) |