Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
4 | g.114623521A>C | CA358002306 | UGT8 | c.641A>C (p.Lys214Thr) | |
4 | g.114623521A>G | CA358002304 | UGT8 | c.641A>G (p.Lys214Arg) | gnomAD v4 |
4 | g.114623521A>T | CA358002305 | UGT8 | c.641A>T (p.Lys214Ile) | |
4 | g.114623522A>C | CA358002307 | UGT8 | c.642A>C (p.Lys214Asn) | |
4 | g.114623522A>G | CA441110489 | UGT8 | c.642A>G (p.Lys214=) | |
4 | g.114623522A>T | CA358002308 | UGT8 | c.642A>T (p.Lys214Asn) | |
4 | g.114623523T>A | CA358002309 | UGT8 | c.643T>A (p.Tyr215Asn) | |
4 | g.114623523T>C | CA358002310 | UGT8 | c.643T>C (p.Tyr215His) | |
4 | g.114623523T>G | CA358002311 | UGT8 | c.643T>G (p.Tyr215Asp) | |
4 | g.114623524A= | CA1486646020 | UGT8 | c.644A= (p.Tyr215=) | |
4 | g.114623524A>C | CA358002312 | UGT8 | c.644A>C (p.Tyr215Ser) | |
4 | g.114623524A>G | CA358002313 | UGT8 | c.644A>G (p.Tyr215Cys) | |
4 | g.114623524A>T | CA358002314 | UGT8 | c.644A>T (p.Tyr215Phe) | dbSNP gnomAD v4 |
4 | g.114623525T>A | CA358002315 | UGT8 | c.645T>A (p.Tyr215Ter) | |
4 | g.114623525T>C | CA441110490 | UGT8 | c.645T>C (p.Tyr215=) | |
4 | g.114623525T>G | CA358002316 | UGT8 | c.645T>G (p.Tyr215Ter) | |
4 | g.114623526G>A | CA358002317 | UGT8 | c.646G>A (p.Glu216Lys) | gnomAD v4 |
4 | g.114623526G>C | CA358002318 | UGT8 | c.646G>C (p.Glu216Gln) | |
4 | g.114623526G= | CA1486646021 | UGT8 | c.646G= (p.Glu216=) | |
4 | g.114623526G>T | CA3053516 | UGT8 | c.646G>T (p.Glu216Ter) | dbSNP ExAC gnomAD v2 gnomAD v4 |
4 | g.114623527A>C | CA358002319 | UGT8 | c.647A>C (p.Glu216Ala) | |
4 | g.114623527A>G | CA358002320 | UGT8 | c.647A>G (p.Glu216Gly) | |
4 | g.114623527A>T | CA358002321 | UGT8 | c.647A>T (p.Glu216Val) | |
4 | g.114623528A>C | CA358002323 | UGT8 | c.648A>C (p.Glu216Asp) | |
4 | g.114623528A>G | CA441110491 | UGT8 | c.648A>G (p.Glu216=) | |
4 | g.114623528A>T | CA358002322 | UGT8 | c.648A>T (p.Glu216Asp) | |
4 | g.114623529A>C | CA441110493 | UGT8 | c.649A>C (p.Arg217=) | |
4 | g.114623529A>G | CA358002324 | UGT8 | c.649A>G (p.Arg217Gly) | |
4 | g.114623529A>T | CA358002325 | UGT8 | c.649A>T (p.Arg217Trp) | |
4 | g.114623530G>A | CA358002326 | UGT8 | c.650G>A (p.Arg217Lys) | gnomAD v4 COSMIC |
4 | g.114623530G>C | CA358002327 | UGT8 | c.650G>C (p.Arg217Thr) | |
4 | g.114623530G>T | CA358002328 | UGT8 | c.650G>T (p.Arg217Met) | |
4 | g.114623531G>A | CA441110494 | UGT8 | c.651G>A (p.Arg217=) | |
4 | g.114623531G>C | CA358002329 | UGT8 | c.651G>C (p.Arg217Ser) | |
4 | g.114623531G= | CA1486646022 | UGT8 | c.651G= (p.Arg217=) | |
4 | g.114623531G>T | CA3053517 | UGT8 | c.651G>T (p.Arg217Ser) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
4 | g.114623532A>C | CA358002330 | UGT8 | c.652A>C (p.Ile218Leu) | |
4 | g.114623532A>G | CA358002332 | UGT8 | c.652A>G (p.Ile218Val) | |
4 | g.114623532A>T | CA358002331 | UGT8 | c.652A>T (p.Ile218Leu) | |
4 | g.114623533T>A | CA358002333 | UGT8 | c.653T>A (p.Ile218Lys) | |
4 | g.114623533T>C | CA358002334 | UGT8 | c.653T>C (p.Ile218Thr) | gnomAD v4 |
4 | g.114623533T>G | CA358002335 | UGT8 | c.653T>G (p.Ile218Arg) | |
4 | g.114623534A= | CA1486646023 | UGT8 | c.654A= (p.Ile218=) | |
4 | g.114623534A>C | CA441110499 | UGT8 | c.654A>C (p.Ile218=) | |
4 | g.114623534A>G | CA3053518 | UGT8 | c.654A>G (p.Ile218Met) | dbSNP ExAC gnomAD v2 gnomAD v4 |
4 | g.114623534A>T | CA441110498 | UGT8 | c.654A>T (p.Ile218=) | gnomAD v4 |
4 | g.114623535A>C | CA358002336 | UGT8 | c.655A>C (p.Met219Leu) | gnomAD v4 |
4 | g.114623535A>G | CA358002338 | UGT8 | c.655A>G (p.Met219Val) | |
4 | g.114623535A>T | CA358002337 | UGT8 | c.655A>T (p.Met219Leu) | |
4 | g.114623536T>A | CA358002339 | UGT8 | c.656T>A (p.Met219Lys) |