Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
4 | g.186603766T>A | CA358976376 | FAT1 | c.10760A>T (p.Asp3587Val) c.10766A>T (p.Asp3589Val) | |
4 | g.186603766T>C | CA358976374 | FAT1 | c.10760A>G (p.Asp3587Gly) c.10766A>G (p.Asp3589Gly) | gnomAD v4 |
4 | g.186603766T>G | CA358976372 | FAT1 | c.10760A>C (p.Asp3587Ala) c.10766A>C (p.Asp3589Ala) | |
4 | g.186603767C>A | CA358976378 | FAT1 | c.10759G>T (p.Asp3587Tyr) c.10765G>T (p.Asp3589Tyr) | dbSNP COSMIC COSMIC |
4 | g.186603767C= | CA1520094215 | FAT1 | c.10759G= (p.Asp3587=) c.10765G= (p.Asp3589=) | |
4 | g.186603767C>G | CA358976380 | FAT1 | c.10759G>C (p.Asp3587His) c.10765G>C (p.Asp3589His) | dbSNP |
4 | g.186603767C>T | CA3165277 | FAT1 | c.10759G>A (p.Asp3587Asn) c.10765G>A (p.Asp3589Asn) | dbSNP ExAC gnomAD v2 gnomAD v4 |
4 | g.186603768C>A | CA358976384 | FAT1 | c.10758G>T (p.Met3586Ile) c.10764G>T (p.Met3588Ile) | dbSNP |
4 | g.186603768C>G | CA358976385 | FAT1 | c.10758G>C (p.Met3586Ile) c.10764G>C (p.Met3588Ile) | dbSNP |
4 | g.186603768C>T | CA358976387 | FAT1 | c.10758G>A (p.Met3586Ile) c.10764G>A (p.Met3588Ile) | dbSNP gnomAD v4 |
4 | g.186603769A= | CA1520094216 | FAT1 | c.10757T= (p.Met3586=) c.10763T= (p.Met3588=) | |
4 | g.186603769A>C | CA358976389 | FAT1 | c.10757T>G (p.Met3586Arg) c.10763T>G (p.Met3588Arg) | dbSNP |
4 | g.186603769A>G | CA3165278 | FAT1 | c.10757T>C (p.Met3586Thr) c.10763T>C (p.Met3588Thr) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
4 | g.186603769A>T | CA358976391 | FAT1 | c.10757T>A (p.Met3586Lys) c.10763T>A (p.Met3588Lys) | dbSNP |
4 | g.186603770T>A | CA358976396 | FAT1 | c.10756A>T (p.Met3586Leu) c.10762A>T (p.Met3588Leu) | dbSNP |
4 | g.186603770T>C | CA358976398 | FAT1 | c.10756A>G (p.Met3586Val) c.10762A>G (p.Met3588Val) | dbSNP gnomAD v4 |
4 | g.186603770T>G | CA358976400 | FAT1 | c.10756A>C (p.Met3586Leu) c.10762A>C (p.Met3588Leu) | |
4 | g.186603771C>A | CA358976402 | FAT1 | c.10755G>T (p.Gln3585His) c.10761G>T (p.Gln3587His) | dbSNP |
4 | g.186603771C>G | CA358976403 | FAT1 | c.10755G>C (p.Gln3585His) c.10761G>C (p.Gln3587His) | dbSNP |
4 | g.186603771C>T | CA442888783 | FAT1 | c.10755G>A (p.Gln3585=) c.10761G>A (p.Gln3587=) | dbSNP |
4 | g.186603772T>A | CA358976407 | FAT1 | c.10754A>T (p.Gln3585Leu) c.10760A>T (p.Gln3587Leu) | dbSNP |
4 | g.186603772T>C | CA358976409 | FAT1 | c.10754A>G (p.Gln3585Arg) c.10760A>G (p.Gln3587Arg) | dbSNP gnomAD v4 |
4 | g.186603772T>G | CA358976411 | FAT1 | c.10754A>C (p.Gln3585Pro) c.10760A>C (p.Gln3587Pro) | |
4 | g.186603773G>A | CA358976413 | FAT1 | c.10753C>T (p.Gln3585Ter) c.10759C>T (p.Gln3587Ter) | dbSNP COSMIC COSMIC |
4 | g.186603773G>C | CA358976416 | FAT1 | c.10753C>G (p.Gln3585Glu) c.10759C>G (p.Gln3587Glu) | dbSNP |
4 | g.186603773G>T | CA358976419 | FAT1 | c.10753C>A (p.Gln3585Lys) c.10759C>A (p.Gln3587Lys) | |
4 | g.186603774A>C | CA442888792 | FAT1 | c.10752T>G (p.Pro3584=) c.10758T>G (p.Pro3586=) | dbSNP gnomAD v4 |
4 | g.186603774A>G | CA442888794 | FAT1 | c.10752T>C (p.Pro3584=) c.10758T>C (p.Pro3586=) | dbSNP |
4 | g.186603774A>T | CA442888796 | FAT1 | c.10752T>A (p.Pro3584=) c.10758T>A (p.Pro3586=) | dbSNP |
4 | g.186603775G>A | CA358976421 | FAT1 | c.10751C>T (p.Pro3584Leu) c.10757C>T (p.Pro3586Leu) | dbSNP |
4 | g.186603775G>C | CA358976424 | FAT1 | c.10751C>G (p.Pro3584Arg) c.10757C>G (p.Pro3586Arg) | dbSNP |
4 | g.186603775G>T | CA358976422 | FAT1 | c.10751C>A (p.Pro3584His) c.10757C>A (p.Pro3586His) | dbSNP |
4 | g.186603776G>A | CA358976427 | FAT1 | c.10750C>T (p.Pro3584Ser) c.10756C>T (p.Pro3586Ser) | dbSNP COSMIC COSMIC |
4 | g.186603776G>C | CA358976429 | FAT1 | c.10750C>G (p.Pro3584Ala) c.10756C>G (p.Pro3586Ala) | dbSNP |
4 | g.186603776G>T | CA358976430 | FAT1 | c.10750C>A (p.Pro3584Thr) c.10756C>A (p.Pro3586Thr) | dbSNP |
4 | g.186603777G>A | CA442888802 | FAT1 | c.10749C>T (p.Asp3583=) c.10755C>T (p.Asp3585=) | dbSNP |
4 | g.186603777G>C | CA358976433 | FAT1 | c.10749C>G (p.Asp3583Glu) c.10755C>G (p.Asp3585Glu) | dbSNP |
4 | g.186603777G>T | CA358976435 | FAT1 | c.10749C>A (p.Asp3583Glu) c.10755C>A (p.Asp3585Glu) | |
4 | g.186603778T>A | CA358976438 | FAT1 | c.10748A>T (p.Asp3583Val) c.10754A>T (p.Asp3585Val) | dbSNP |
4 | g.186603778T>C | CA358976440 | FAT1 | c.10748A>G (p.Asp3583Gly) c.10754A>G (p.Asp3585Gly) | dbSNP |
4 | g.186603778T>G | CA358976441 | FAT1 | c.10748A>C (p.Asp3583Ala) c.10754A>C (p.Asp3585Ala) | dbSNP |
4 | g.186603779C>A | CA112157380 | FAT1 | c.10747G>T (p.Asp3583Tyr) c.10753G>T (p.Asp3585Tyr) | dbSNP gnomAD v4 |
4 | g.186603779C= | CA1520094217 | FAT1 | c.10747G= (p.Asp3583=) c.10753G= (p.Asp3585=) | |
4 | g.186603779C>G | CA358976446 | FAT1 | c.10747G>C (p.Asp3583His) c.10753G>C (p.Asp3585His) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
4 | g.186603779C>T | CA3165279 | FAT1 | c.10747G>A (p.Asp3583Asn) c.10753G>A (p.Asp3585Asn) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC COSMIC |
4 | g.186603780G>A | CA3165280 | FAT1 | c.10746C>T (p.Leu3582=) c.10752C>T (p.Leu3584=) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
4 | g.186603780G>C | CA442888813 | FAT1 | c.10746C>G (p.Leu3582=) c.10752C>G (p.Leu3584=) | dbSNP |
4 | g.186603780G= | CA1520094218 | FAT1 | c.10746C= (p.Leu3582=) c.10752C= (p.Leu3584=) | |
4 | g.186603780G>T | CA442888814 | FAT1 | c.10746C>A (p.Leu3582=) c.10752C>A (p.Leu3584=) | dbSNP |
4 | g.186603781A>C | CA358976454 | FAT1 | c.10745T>G (p.Leu3582Arg) c.10751T>G (p.Leu3584Arg) |