UPDATE - Protein Allele ID & Protein Sequence HGVS Requests Partially Restored
Protein allele requests are no longer disabled.
Currently, hypothetical explanatory transcript generation is not part of the response and is being investigated.
Protein allele requests are no longer disabled.
Currently, hypothetical explanatory transcript generation is not part of the response and is being investigated.
| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 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) | |
| 4 | g.186603781A>G | CA358976450 | FAT1 | c.10745T>C (p.Leu3582Pro) c.10751T>C (p.Leu3584Pro) | dbSNP |
| 4 | g.186603781A>T | CA358976452 | FAT1 | c.10745T>A (p.Leu3582His) c.10751T>A (p.Leu3584His) | dbSNP |
| 4 | g.186603782G>A | CA358976457 | FAT1 | c.10744C>T (p.Leu3582Phe) c.10750C>T (p.Leu3584Phe) | dbSNP |
| 4 | g.186603782G>C | CA358976459 | FAT1 | c.10744C>G (p.Leu3582Val) c.10750C>G (p.Leu3584Val) | dbSNP |
| 4 | g.186603782G>T | CA358976461 | FAT1 | c.10744C>A (p.Leu3582Ile) c.10750C>A (p.Leu3584Ile) | dbSNP |
| 4 | g.186603783A>C | CA358976464 | FAT1 | c.10743T>G (p.Ser3581Arg) c.10749T>G (p.Ser3583Arg) | dbSNP |
| 4 | g.186603783A>G | CA442888824 | FAT1 | c.10743T>C (p.Ser3581=) c.10749T>C (p.Ser3583=) | dbSNP |
| 4 | g.186603783A>T | CA358976466 | FAT1 | c.10743T>A (p.Ser3581Arg) c.10749T>A (p.Ser3583Arg) | dbSNP |
| 4 | g.186603784C>A | CA358976468 | FAT1 | c.10742G>T (p.Ser3581Ile) c.10748G>T (p.Ser3583Ile) | dbSNP |
| 4 | g.186603784C>G | CA358976470 | FAT1 | c.10742G>C (p.Ser3581Thr) c.10748G>C (p.Ser3583Thr) | dbSNP |
| 4 | g.186603784C>T | CA358976472 | FAT1 | c.10742G>A (p.Ser3581Asn) c.10748G>A (p.Ser3583Asn) | dbSNP |
| 4 | g.186603784_186603790dup | CA2672910505 | FAT1 | c.10736_10742dup (p.Asp3583GlnfsTer?) c.10742_10748dup (p.Asp3585GlnfsTer?) | gnomAD v4 |
| 4 | g.186603785T>A | CA358976474 | FAT1 | c.10741A>T (p.Ser3581Cys) c.10747A>T (p.Ser3583Cys) | dbSNP |
| 4 | g.186603785T>C | CA358976475 | FAT1 | c.10741A>G (p.Ser3581Gly) c.10747A>G (p.Ser3583Gly) | |
| 4 | g.186603785T>G | CA358976476 | FAT1 | c.10741A>C (p.Ser3581Arg) c.10747A>C (p.Ser3583Arg) | |
| 4 | g.186603786G>A | CA3165281 | FAT1 | c.10740C>T (p.Tyr3580=) c.10746C>T (p.Tyr3582=) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 4 | g.186603786G>C | CA358976482 | FAT1 | c.10740C>G (p.Tyr3580Ter) c.10746C>G (p.Tyr3582Ter) | dbSNP |
| 4 | g.186603786G= | CA1520094219 | FAT1 | c.10740C= (p.Tyr3580=) c.10746C= (p.Tyr3582=) | |
| 4 | g.186603786G>T | CA358976479 | FAT1 | c.10740C>A (p.Tyr3580Ter) c.10746C>A (p.Tyr3582Ter) | |
| 4 | g.186603787T>A | CA358976495 | FAT1 | c.10739A>T (p.Tyr3580Phe) c.10745A>T (p.Tyr3582Phe) | dbSNP |
| 4 | g.186603787T>C | CA358976491 | FAT1 | c.10739A>G (p.Tyr3580Cys) c.10745A>G (p.Tyr3582Cys) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 4 | g.186603787T>G | CA358976493 | FAT1 | c.10739A>C (p.Tyr3580Ser) c.10745A>C (p.Tyr3582Ser) | dbSNP |
| 4 | g.186603787T= | CA1520094220 | FAT1 | c.10739A= (p.Tyr3580=) c.10745A= (p.Tyr3582=) | |
| 4 | g.186603788A= | CA1520094221 | FAT1 | c.10738T= (p.Tyr3580=) c.10744T= (p.Tyr3582=) | |
| 4 | g.186603788A>C | CA358976497 | FAT1 | c.10738T>G (p.Tyr3580Asp) c.10744T>G (p.Tyr3582Asp) | |
| 4 | g.186603788A>G | CA358976499 | FAT1 | c.10738T>C (p.Tyr3580His) c.10744T>C (p.Tyr3582His) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 4 | g.186603788A>T | CA358976501 | FAT1 | c.10738T>A (p.Tyr3580Asn) c.10744T>A (p.Tyr3582Asn) | dbSNP |
| 4 | g.186603789G>A | CA442888843 | FAT1 | c.10737C>T (p.Thr3579=) c.10743C>T (p.Thr3581=) | dbSNP gnomAD v2 gnomAD v4 |
| 4 | g.186603789G>C | CA442888845 | FAT1 | c.10737C>G (p.Thr3579=) c.10743C>G (p.Thr3581=) | dbSNP |
| 4 | g.186603789G= | CA1520094222 | FAT1 | c.10737C= (p.Thr3579=) c.10743C= (p.Thr3581=) | |
| 4 | g.186603789G>T | CA442888847 | FAT1 | c.10737C>A (p.Thr3579=) c.10743C>A (p.Thr3581=) | dbSNP gnomAD v4 COSMIC COSMIC |
| 4 | g.186603790G>A | CA358976504 | FAT1 | c.10736C>T (p.Thr3579Ile) c.10742C>T (p.Thr3581Ile) | gnomAD v4 |
| 4 | g.186603790G>C | CA358976506 | FAT1 | c.10736C>G (p.Thr3579Ser) c.10742C>G (p.Thr3581Ser) | gnomAD v4 |
| 4 | g.186603790G>T | CA358976508 | FAT1 | c.10736C>A (p.Thr3579Asn) c.10742C>A (p.Thr3581Asn) | |
| 4 | g.186603791T>A | CA358976510 | FAT1 | c.10735A>T (p.Thr3579Ser) c.10741A>T (p.Thr3581Ser) | dbSNP gnomAD v4 |
| 4 | g.186603791T>C | CA358976512 | FAT1 | c.10735A>G (p.Thr3579Ala) c.10741A>G (p.Thr3581Ala) | dbSNP |
| 4 | g.186603791T>G | CA358976514 | FAT1 | c.10735A>C (p.Thr3579Pro) c.10741A>C (p.Thr3581Pro) | dbSNP |
| 4 | g.186603792T>A | CA442888858 | FAT1 | c.10734A>T (p.Leu3578=) c.10740A>T (p.Leu3580=) | dbSNP |
| 4 | g.186603792T>C | CA442888856 | FAT1 | c.10734A>G (p.Leu3578=) c.10740A>G (p.Leu3580=) | dbSNP gnomAD v2 gnomAD v4 |
| 4 | g.186603792T>G | CA442888855 | FAT1 | c.10734A>C (p.Leu3578=) c.10740A>C (p.Leu3580=) | dbSNP |
| 4 | g.186603792T= | CA1520094223 | FAT1 | c.10734A= (p.Leu3578=) c.10740A= (p.Leu3580=) | |
| 4 | g.186603793A>C | CA358976520 | FAT1 | c.10733T>G (p.Leu3578Arg) c.10739T>G (p.Leu3580Arg) | |
| 4 | g.186603793A>G | CA358976518 | FAT1 | c.10733T>C (p.Leu3578Pro) c.10739T>C (p.Leu3580Pro) | dbSNP |
| 4 | g.186603793A>T | CA358976516 | FAT1 | c.10733T>A (p.Leu3578Gln) c.10739T>A (p.Leu3580Gln) | dbSNP |
| 4 | g.186603794G>A | CA442888864 | FAT1 | c.10732C>T (p.Leu3578=) c.10738C>T (p.Leu3580=) | dbSNP |
| 4 | g.186603794G>C | CA358976523 | FAT1 | c.10732C>G (p.Leu3578Val) c.10738C>G (p.Leu3580Val) | dbSNP |
| 4 | g.186603794G>T | CA358976525 | FAT1 | c.10732C>A (p.Leu3578Ile) c.10738C>A (p.Leu3580Ile) | |
| 4 | g.186603795A>C | CA442888867 | FAT1 | c.10731T>G (p.Thr3577=) c.10737T>G (p.Thr3579=) | |
| 4 | g.186603795A>G | CA442888869 | FAT1 | c.10731T>C (p.Thr3577=) c.10737T>C (p.Thr3579=) | gnomAD v4 |
| 4 | g.186603795A>T | CA442888870 | FAT1 | c.10731T>A (p.Thr3577=) c.10737T>A (p.Thr3579=) | dbSNP |
| 4 | g.186603796G>A | CA358976528 | FAT1 | c.10730C>T (p.Thr3577Ile) c.10736C>T (p.Thr3579Ile) | dbSNP |
| 4 | g.186603796G>C | CA358976530 | FAT1 | c.10730C>G (p.Thr3577Ser) c.10736C>G (p.Thr3579Ser) | dbSNP |
| 4 | g.186603796G= | CA1520094224 | FAT1 | c.10730C= (p.Thr3577=) c.10736C= (p.Thr3579=) | |
| 4 | g.186603796G>T | CA358976532 | FAT1 | c.10730C>A (p.Thr3577Asn) c.10736C>A (p.Thr3579Asn) | dbSNP gnomAD v2 gnomAD v4 |
| 4 | g.186603797T>A | CA358976535 | FAT1 | c.10729A>T (p.Thr3577Ser) c.10735A>T (p.Thr3579Ser) | dbSNP gnomAD v3 gnomAD v4 |
| 4 | g.186603797T>C | CA3165282 | FAT1 | c.10729A>G (p.Thr3577Ala) c.10735A>G (p.Thr3579Ala) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 4 | g.186603797T>G | CA358976538 | FAT1 | c.10729A>C (p.Thr3577Pro) c.10735A>C (p.Thr3579Pro) | dbSNP |
| 4 | g.186603797T= | CA1520094225 | FAT1 | c.10729A= (p.Thr3577=) c.10735A= (p.Thr3579=) | |
| 4 | g.186603798A= | CA1520094226 | FAT1 | c.10728T= (p.Asp3576=) c.10734T= (p.Asp3578=) | |
| 4 | g.186603798A>C | CA358976541 | FAT1 | c.10728T>G (p.Asp3576Glu) c.10734T>G (p.Asp3578Glu) | dbSNP gnomAD v3 gnomAD v4 |
| 4 | g.186603798A>G | CA442888879 | FAT1 | c.10728T>C (p.Asp3576=) c.10734T>C (p.Asp3578=) | |
| 4 | g.186603798A>T | CA358976543 | FAT1 | c.10728T>A (p.Asp3576Glu) c.10734T>A (p.Asp3578Glu) | dbSNP |
| 4 | g.186603799T>A | CA358976546 | FAT1 | c.10727A>T (p.Asp3576Val) c.10733A>T (p.Asp3578Val) | dbSNP |
| 4 | g.186603799T>C | CA358976548 | FAT1 | c.10727A>G (p.Asp3576Gly) c.10733A>G (p.Asp3578Gly) | dbSNP gnomAD v2 gnomAD v4 |
| 4 | g.186603799T>G | CA358976550 | FAT1 | c.10727A>C (p.Asp3576Ala) c.10733A>C (p.Asp3578Ala) | |
| 4 | g.186603799T= | CA1520094227 | FAT1 | c.10727A= (p.Asp3576=) c.10733A= (p.Asp3578=) | |
| 4 | g.186603800C>A | CA358976556 | FAT1 | c.10726G>T (p.Asp3576Tyr) c.10732G>T (p.Asp3578Tyr) | |
| 4 | g.186603800C>G | CA358976558 | FAT1 | c.10726G>C (p.Asp3576His) c.10732G>C (p.Asp3578His) | dbSNP |
| 4 | g.186603800C>T | CA358976553 | FAT1 | c.10726G>A (p.Asp3576Asn) c.10732G>A (p.Asp3578Asn) | dbSNP |
| 4 | g.186603801A>C | CA358976562 | FAT1 | c.10725T>G (p.Tyr3575Ter) c.10731T>G (p.Tyr3577Ter) | |
| 4 | g.186603801A>G | CA442888889 | FAT1 | c.10725T>C (p.Tyr3575=) c.10731T>C (p.Tyr3577=) | gnomAD v4 |
| 4 | g.186603801A>T | CA358976563 | FAT1 | c.10725T>A (p.Tyr3575Ter) c.10731T>A (p.Tyr3577Ter) | dbSNP |
| 4 | g.186603802T>A | CA358976564 | FAT1 | c.10724A>T (p.Tyr3575Phe) c.10730A>T (p.Tyr3577Phe) | dbSNP |
| 4 | g.186603802T>C | CA358976565 | FAT1 | c.10724A>G (p.Tyr3575Cys) c.10730A>G (p.Tyr3577Cys) | dbSNP gnomAD v4 |
| 4 | g.186603802T>G | CA358976567 | FAT1 | c.10724A>C (p.Tyr3575Ser) c.10730A>C (p.Tyr3577Ser) | dbSNP |
| 4 | g.186603803A= | CA1520094228 | FAT1 | c.10723T= (p.Tyr3575=) c.10729T= (p.Tyr3577=) | |
| 4 | g.186603803A>C | CA358976573 | FAT1 | c.10723T>G (p.Tyr3575Asp) c.10729T>G (p.Tyr3577Asp) | dbSNP |
| 4 | g.186603803A>G | CA3165283 | FAT1 | c.10723T>C (p.Tyr3575His) c.10729T>C (p.Tyr3577His) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 4 | g.186603803A>T | CA358976570 | FAT1 | c.10723T>A (p.Tyr3575Asn) c.10729T>A (p.Tyr3577Asn) | dbSNP |
| 4 | g.186603804C>A | CA442888897 | FAT1 | c.10722G>T (p.Val3574=) c.10728G>T (p.Val3576=) | dbSNP |
| 4 | g.186603804C>G | CA442888899 | FAT1 | c.10722G>C (p.Val3574=) c.10728G>C (p.Val3576=) | dbSNP |
| 4 | g.186603804C>T | CA442888901 | FAT1 | c.10722G>A (p.Val3574=) c.10728G>A (p.Val3576=) | dbSNP |
| 4 | g.186603805A>C | CA358976576 | FAT1 | c.10721T>G (p.Val3574Gly) c.10727T>G (p.Val3576Gly) | dbSNP |
| 4 | g.186603805A>G | CA358976578 | FAT1 | c.10721T>C (p.Val3574Ala) c.10727T>C (p.Val3576Ala) | dbSNP |
| 4 | g.186603805A>T | CA358976580 | FAT1 | c.10721T>A (p.Val3574Glu) c.10727T>A (p.Val3576Glu) | dbSNP |
| 4 | g.186603806C>A | CA358976582 | FAT1 | c.10720G>T (p.Val3574Leu) c.10726G>T (p.Val3576Leu) | dbSNP |
| 4 | g.186603806C= | CA1520094229 | FAT1 | c.10720G= (p.Val3574=) c.10726G= (p.Val3576=) | |
| 4 | g.186603806C>G | CA358976584 | FAT1 | c.10720G>C (p.Val3574Leu) c.10726G>C (p.Val3576Leu) | dbSNP |
| 4 | g.186603806C>T | CA3165284 | FAT1 | c.10720G>A (p.Val3574Met) c.10726G>A (p.Val3576Met) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
| 4 | g.186603807G>A | CA3165285 | FAT1 | c.10719C>T (p.Asp3573=) c.10725C>T (p.Asp3575=) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 4 | g.186603807G>C | CA358976591 | FAT1 | c.10719C>G (p.Asp3573Glu) c.10725C>G (p.Asp3575Glu) | dbSNP |
| 4 | g.186603807G= | CA1520094230 | FAT1 | c.10719C= (p.Asp3573=) c.10725C= (p.Asp3575=) | |
| 4 | g.186603807G>T | CA358976589 | FAT1 | c.10719C>A (p.Asp3573Glu) c.10725C>A (p.Asp3575Glu) | gnomAD v4 |
| 4 | g.186603808T>A | CA358976594 | FAT1 | c.10718A>T (p.Asp3573Val) c.10724A>T (p.Asp3575Val) | dbSNP |
| 4 | g.186603808T>C | CA358976596 | FAT1 | c.10718A>G (p.Asp3573Gly) c.10724A>G (p.Asp3575Gly) | dbSNP |
| 4 | g.186603808T>G | CA358976597 | FAT1 | c.10718A>C (p.Asp3573Ala) c.10724A>C (p.Asp3575Ala) | dbSNP |
| 4 | g.186603809C>A | CA358976599 | FAT1 | c.10717G>T (p.Asp3573Tyr) c.10723G>T (p.Asp3575Tyr) | dbSNP |
| 4 | g.186603809C>G | CA358976601 | FAT1 | c.10717G>C (p.Asp3573His) c.10723G>C (p.Asp3575His) | dbSNP |
| 4 | g.186603809C>T | CA358976603 | FAT1 | c.10717G>A (p.Asp3573Asn) c.10723G>A (p.Asp3575Asn) | dbSNP |
| 4 | g.186603810C>A | CA358976605 | FAT1 | c.10716G>T (p.Gln3572His) c.10722G>T (p.Gln3574His) | dbSNP |
| 4 | g.186603810C= | CA1520094231 | FAT1 | c.10716G= (p.Gln3572=) c.10722G= (p.Gln3574=) | |
| 4 | g.186603810C>G | CA358976607 | FAT1 | c.10716G>C (p.Gln3572His) c.10722G>C (p.Gln3574His) | dbSNP |
| 4 | g.186603810C>T | CA3165286 | FAT1 | c.10716G>A (p.Gln3572=) c.10722G>A (p.Gln3574=) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 4 | g.186603811T>A | CA358976610 | FAT1 | c.10715A>T (p.Gln3572Leu) c.10721A>T (p.Gln3574Leu) | |
| 4 | g.186603811T>C | CA358976612 | FAT1 | c.10715A>G (p.Gln3572Arg) c.10721A>G (p.Gln3574Arg) | |
| 4 | g.186603811T>G | CA358976615 | FAT1 | c.10715A>C (p.Gln3572Pro) c.10721A>C (p.Gln3574Pro) | |
| 4 | g.186603812G>A | CA358976621 | FAT1 | c.10714C>T (p.Gln3572Ter) c.10720C>T (p.Gln3574Ter) | dbSNP |
| 4 | g.186603812G>C | CA358976619 | FAT1 | c.10714C>G (p.Gln3572Glu) c.10720C>G (p.Gln3574Glu) | dbSNP gnomAD v4 |
| 4 | g.186603812G>T | CA358976618 | FAT1 | c.10714C>A (p.Gln3572Lys) c.10720C>A (p.Gln3574Lys) | dbSNP gnomAD v4 |
| 4 | g.186603813G>A | CA442888927 | FAT1 | c.10713C>T (p.Asp3571=) c.10719C>T (p.Asp3573=) | dbSNP |
| 4 | g.186603813G>C | CA358976625 | FAT1 | c.10713C>G (p.Asp3571Glu) c.10719C>G (p.Asp3573Glu) | dbSNP |
| 4 | g.186603813G>T | CA358976627 | FAT1 | c.10713C>A (p.Asp3571Glu) c.10719C>A (p.Asp3573Glu) | dbSNP |
| 4 | g.186603814T>A | CA358976630 | FAT1 | c.10712A>T (p.Asp3571Val) c.10718A>T (p.Asp3573Val) | dbSNP |
| 4 | g.186603814T>C | CA358976632 | FAT1 | c.10712A>G (p.Asp3571Gly) c.10718A>G (p.Asp3573Gly) | dbSNP |
| 4 | g.186603814T>G | CA358976634 | FAT1 | c.10712A>C (p.Asp3571Ala) c.10718A>C (p.Asp3573Ala) | |
| 4 | g.186603815C>A | CA358976637 | FAT1 | c.10711G>T (p.Asp3571Tyr) c.10717G>T (p.Asp3573Tyr) | dbSNP |
| 4 | g.186603815C>G | CA358976639 | FAT1 | c.10711G>C (p.Asp3571His) c.10717G>C (p.Asp3573His) | dbSNP |
| 4 | g.186603815C>T | CA358976641 | FAT1 | c.10711G>A (p.Asp3571Asn) c.10717G>A (p.Asp3573Asn) | dbSNP |
| 4 | g.186603816T>A | CA442888937 | FAT1 | c.10710A>T (p.Thr3570=) c.10716A>T (p.Thr3572=) | dbSNP |
| 4 | g.186603816T>C | CA442888938 | FAT1 | c.10710A>G (p.Thr3570=) c.10716A>G (p.Thr3572=) | dbSNP |
| 4 | g.186603816T>G | CA442888941 | FAT1 | c.10710A>C (p.Thr3570=) c.10716A>C (p.Thr3572=) | |
| 4 | g.186603817G>A | CA358976644 | FAT1 | c.10709C>T (p.Thr3570Ile) c.10715C>T (p.Thr3572Ile) | dbSNP COSMIC COSMIC |
| 4 | g.186603817G>C | CA358976648 | FAT1 | c.10709C>G (p.Thr3570Arg) c.10715C>G (p.Thr3572Arg) | dbSNP |
| 4 | g.186603817G>T | CA358976645 | FAT1 | c.10709C>A (p.Thr3570Lys) c.10715C>A (p.Thr3572Lys) | |
| 4 | g.186603818T>A | CA358976650 | FAT1 | c.10708A>T (p.Thr3570Ser) c.10714A>T (p.Thr3572Ser) | dbSNP |
| 4 | g.186603818T>C | CA358976652 | FAT1 | c.10708A>G (p.Thr3570Ala) c.10714A>G (p.Thr3572Ala) | gnomAD v4 |
| 4 | g.186603818T>G | CA358976654 | FAT1 | c.10708A>C (p.Thr3570Pro) c.10714A>C (p.Thr3572Pro) | |
| 4 | g.186603819G>A | CA3165287 | FAT1 | c.10707C>T (p.Ala3569=) c.10713C>T (p.Ala3571=) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 4 | g.186603819G>C | CA442888949 | FAT1 | c.10707C>G (p.Ala3569=) c.10713C>G (p.Ala3571=) | |
| 4 | g.186603819G= | CA1520094232 | FAT1 | c.10707C= (p.Ala3569=) c.10713C= (p.Ala3571=) | |
| 4 | g.186603819G>T | CA442888952 | FAT1 | c.10707C>A (p.Ala3569=) c.10713C>A (p.Ala3571=) | |
| 4 | g.186603820G>A | CA358976662 | FAT1 | c.10706C>T (p.Ala3569Val) c.10712C>T (p.Ala3571Val) | dbSNP |
| 4 | g.186603820G>C | CA358976659 | FAT1 | c.10706C>G (p.Ala3569Gly) c.10712C>G (p.Ala3571Gly) | |
| 4 | g.186603820G>T | CA358976660 | FAT1 | c.10706C>A (p.Ala3569Asp) c.10712C>A (p.Ala3571Asp) | COSMIC COSMIC |
| 4 | g.186603821C>A | CA358976665 | FAT1 | c.10705G>T (p.Ala3569Ser) c.10711G>T (p.Ala3571Ser) | dbSNP |
| 4 | g.186603821C>G | CA358976668 | FAT1 | c.10705G>C (p.Ala3569Pro) c.10711G>C (p.Ala3571Pro) | dbSNP |
| 4 | g.186603821C>T | CA358976670 | FAT1 | c.10705G>A (p.Ala3569Thr) c.10711G>A (p.Ala3571Thr) | dbSNP |
| 4 | g.186603822A= | CA1520094233 | FAT1 | c.10704T= (p.His3568=) c.10710T= (p.His3570=) | |
| 4 | g.186603822A>C | CA358976673 | FAT1 | c.10704T>G (p.His3568Gln) c.10710T>G (p.His3570Gln) | |
| 4 | g.186603822A>G | CA3165288 | FAT1 | c.10704T>C (p.His3568=) c.10710T>C (p.His3570=) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 4 | g.186603822A>T | CA358976675 | FAT1 | c.10704T>A (p.His3568Gln) c.10710T>A (p.His3570Gln) | dbSNP |
| 4 | g.186603823T>A | CA358976678 | FAT1 | c.10703A>T (p.His3568Leu) c.10709A>T (p.His3570Leu) | |
| 4 | g.186603823T>C | CA358976680 | FAT1 | c.10703A>G (p.His3568Arg) c.10709A>G (p.His3570Arg) | gnomAD v4 |
| 4 | g.186603823T>G | CA358976683 | FAT1 | c.10703A>C (p.His3568Pro) c.10709A>C (p.His3570Pro) | |
| 4 | g.186603824G>A | CA358976684 | FAT1 | c.10702C>T (p.His3568Tyr) c.10708C>T (p.His3570Tyr) | dbSNP |
| 4 | g.186603824G>C | CA358976686 | FAT1 | c.10702C>G (p.His3568Asp) c.10708C>G (p.His3570Asp) | dbSNP |
| 4 | g.186603824G>T | CA358976688 | FAT1 | c.10702C>A (p.His3568Asn) c.10708C>A (p.His3570Asn) | dbSNP |
| 4 | g.186603825G>A | CA442888969 | FAT1 | c.10701C>T (p.Ile3567=) c.10707C>T (p.Ile3569=) | dbSNP |
| 4 | g.186603825G>C | CA358976691 | FAT1 | c.10701C>G (p.Ile3567Met) c.10707C>G (p.Ile3569Met) | ClinVar dbSNP gnomAD v4 |
| 4 | g.186603825G= | CA1520094234 | FAT1 | c.10701C= (p.Ile3567=) c.10707C= (p.Ile3569=) | |
| 4 | g.186603825G>T | CA442888972 | FAT1 | c.10701C>A (p.Ile3567=) c.10707C>A (p.Ile3569=) | dbSNP |
| 4 | g.186603826A>C | CA358976697 | FAT1 | c.10700T>G (p.Ile3567Ser) c.10706T>G (p.Ile3569Ser) | dbSNP |
| 4 | g.186603826A>G | CA358976693 | FAT1 | c.10700T>C (p.Ile3567Thr) c.10706T>C (p.Ile3569Thr) | |
| 4 | g.186603826A>T | CA358976695 | FAT1 | c.10700T>A (p.Ile3567Asn) c.10706T>A (p.Ile3569Asn) | dbSNP |
| 4 | g.186603827T>A | CA358976700 | FAT1 | c.10699A>T (p.Ile3567Phe) c.10705A>T (p.Ile3569Phe) | dbSNP |
| 4 | g.186603827T>C | CA358976702 | FAT1 | c.10699A>G (p.Ile3567Val) c.10705A>G (p.Ile3569Val) | dbSNP |
| 4 | g.186603827T>G | CA358976704 | FAT1 | c.10699A>C (p.Ile3567Leu) c.10705A>C (p.Ile3569Leu) | dbSNP |
| 4 | g.186603828C>A | CA358976707 | FAT1 | c.10698G>T (p.Lys3566Asn) c.10704G>T (p.Lys3568Asn) | gnomAD v4 |
| 4 | g.186603828C>G | CA358976709 | FAT1 | c.10698G>C (p.Lys3566Asn) c.10704G>C (p.Lys3568Asn) | |
| 4 | g.186603828C>T | CA442888982 | FAT1 | c.10698G>A (p.Lys3566=) c.10704G>A (p.Lys3568=) | |
| 4 | g.186603829T>A | CA358976716 | FAT1 | c.10697A>T (p.Lys3566Met) c.10703A>T (p.Lys3568Met) | dbSNP |
| 4 | g.186603829T>C | CA358976714 | FAT1 | c.10697A>G (p.Lys3566Arg) c.10703A>G (p.Lys3568Arg) | |
| 4 | g.186603829T>G | CA358976712 | FAT1 | c.10697A>C (p.Lys3566Thr) c.10703A>C (p.Lys3568Thr) | |
| 4 | g.186603830T>A | CA358976720 | FAT1 | c.10696A>T (p.Lys3566Ter) c.10702A>T (p.Lys3568Ter) | |
| 4 | g.186603830T>C | CA358976721 | FAT1 | c.10696A>G (p.Lys3566Glu) c.10702A>G (p.Lys3568Glu) | |
| 4 | g.186603830T>G | CA358976724 | FAT1 | c.10696A>C (p.Lys3566Gln) c.10702A>C (p.Lys3568Gln) | COSMIC COSMIC |
| 4 | g.186603830_186603832del | CA1072009921 | FAT1 | c.10694_10696del (p.Gly3565_Lys3566delinsGlu) c.10700_10702del (p.Gly3567_Lys3568delinsGlu) | gnomAD v3 gnomAD v4 |
| 4 | g.186603831C>A | CA442888991 | FAT1 | c.10695G>T (p.Gly3565=) c.10701G>T (p.Gly3567=) | dbSNP |
| 4 | g.186603831C>G | CA442888993 | FAT1 | c.10695G>C (p.Gly3565=) c.10701G>C (p.Gly3567=) | dbSNP |
| 4 | g.186603831C>T | CA442888995 | FAT1 | c.10695G>A (p.Gly3565=) c.10701G>A (p.Gly3567=) | dbSNP |
| 4 | g.186603832C>A | CA358976726 | FAT1 | c.10694G>T (p.Gly3565Val) c.10700G>T (p.Gly3567Val) | dbSNP |
| 4 | g.186603832C>G | CA358976728 | FAT1 | c.10694G>C (p.Gly3565Ala) c.10700G>C (p.Gly3567Ala) | dbSNP |
| 4 | g.186603832C>T | CA358976730 | FAT1 | c.10694G>A (p.Gly3565Glu) c.10700G>A (p.Gly3567Glu) | dbSNP |
| 4 | g.186603833C>A | CA358976737 | FAT1 | c.10693G>T (p.Gly3565Trp) c.10699G>T (p.Gly3567Trp) | dbSNP |
| 4 | g.186603833C>G | CA358976733 | FAT1 | c.10693G>C (p.Gly3565Arg) c.10699G>C (p.Gly3567Arg) | dbSNP |
| 4 | g.186603833C>T | CA358976735 | FAT1 | c.10693G>A (p.Gly3565Arg) c.10699G>A (p.Gly3567Arg) | dbSNP |
| 4 | g.186603834A= | CA1520094235 | FAT1 | c.10692T= (p.Ile3564=) c.10698T= (p.Ile3566=) | |
| 4 | g.186603834A>C | CA358976739 | FAT1 | c.10692T>G (p.Ile3564Met) c.10698T>G (p.Ile3566Met) | |
| 4 | g.186603834A>G | CA442889018 | FAT1 | c.10692T>C (p.Ile3564=) c.10698T>C (p.Ile3566=) | gnomAD v3 gnomAD v4 |
| 4 | g.186603834A>T | CA3165289 | FAT1 | c.10692T>A (p.Ile3564=) c.10698T>A (p.Ile3566=) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 4 | g.186603835A= | CA1520094236 | FAT1 | c.10691T= (p.Ile3564=) c.10697T= (p.Ile3566=) | |
| 4 | g.186603835A>C | CA358976743 | FAT1 | c.10691T>G (p.Ile3564Ser) c.10697T>G (p.Ile3566Ser) | dbSNP |
| 4 | g.186603835A>G | CA358976745 | FAT1 | c.10691T>C (p.Ile3564Thr) c.10697T>C (p.Ile3566Thr) | dbSNP gnomAD v3 gnomAD v4 |
| 4 | g.186603835A>T | CA358976747 | FAT1 | c.10691T>A (p.Ile3564Asn) c.10697T>A (p.Ile3566Asn) | dbSNP |
| 4 | g.186603836T>A | CA358976750 | FAT1 | c.10690A>T (p.Ile3564Phe) c.10696A>T (p.Ile3566Phe) | dbSNP |
| 4 | g.186603836T>C | CA358976751 | FAT1 | c.10690A>G (p.Ile3564Val) c.10696A>G (p.Ile3566Val) | |
| 4 | g.186603836T>G | CA358976754 | FAT1 | c.10690A>C (p.Ile3564Leu) c.10696A>C (p.Ile3566Leu) | dbSNP |
| 4 | g.186603837G>A | CA3165290 | FAT1 | c.10689C>T (p.Val3563=) c.10695C>T (p.Val3565=) | dbSNP ExAC gnomAD v2 gnomAD v4 COSMIC COSMIC |
| 4 | g.186603837G>C | CA442889030 | FAT1 | c.10689C>G (p.Val3563=) c.10695C>G (p.Val3565=) | dbSNP |
| 4 | g.186603837G= | CA1520094237 | FAT1 | c.10689C= (p.Val3563=) c.10695C= (p.Val3565=) | |
| 4 | g.186603837G>T | CA442889033 | FAT1 | c.10689C>A (p.Val3563=) c.10695C>A (p.Val3565=) | dbSNP |
| 4 | g.186603837dup | CA1072009929 | FAT1 | c.10689dup (p.Ile3564HisfsTer13) c.10695dup (p.Ile3566HisfsTer13) | gnomAD v3 gnomAD v4 |
| 4 | g.186603838A>C | CA358976757 | FAT1 | c.10688T>G (p.Val3563Gly) c.10694T>G (p.Val3565Gly) | dbSNP |
| 4 | g.186603838A>G | CA358976759 | FAT1 | c.10688T>C (p.Val3563Ala) c.10694T>C (p.Val3565Ala) | dbSNP COSMIC COSMIC |
| 4 | g.186603838A>T | CA358976762 | FAT1 | c.10688T>A (p.Val3563Asp) c.10694T>A (p.Val3565Asp) | dbSNP gnomAD v3 gnomAD v4 |
| 4 | g.186603839C>A | CA358976764 | FAT1 | c.10687G>T (p.Val3563Phe) c.10693G>T (p.Val3565Phe) | |
| 4 | g.186603839C= | CA1520094238 | FAT1 | c.10687G= (p.Val3563=) c.10693G= (p.Val3565=) | |
| 4 | g.186603839C>G | CA358976767 | FAT1 | c.10687G>C (p.Val3563Leu) c.10693G>C (p.Val3565Leu) | dbSNP |
| 4 | g.186603839C>T | CA3165291 | FAT1 | c.10687G>A (p.Val3563Ile) c.10693G>A (p.Val3565Ile) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 4 | g.186603840G>A | CA442889045 | FAT1 | c.10686C>T (p.Gly3562=) c.10692C>T (p.Gly3564=) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 4 | g.186603840G>C | CA442889047 | FAT1 | c.10686C>G (p.Gly3562=) c.10692C>G (p.Gly3564=) | |
| 4 | g.186603840G= | CA1520094239 | FAT1 | c.10686C= (p.Gly3562=) c.10692C= (p.Gly3564=) | |
| 4 | g.186603840G>T | CA442889049 | FAT1 | c.10686C>A (p.Gly3562=) c.10692C>A (p.Gly3564=) | |
| 4 | g.186603841C>A | CA358976770 | FAT1 | c.10685G>T (p.Gly3562Val) c.10691G>T (p.Gly3564Val) | dbSNP |
| 4 | g.186603841C= | CA1520094240 | FAT1 | c.10685G= (p.Gly3562=) c.10691G= (p.Gly3564=) | |
| 4 | g.186603841C>G | CA358976773 | FAT1 | c.10685G>C (p.Gly3562Ala) c.10691G>C (p.Gly3564Ala) | dbSNP |
| 4 | g.186603841C>T | CA358976775 | FAT1 | c.10685G>A (p.Gly3562Asp) c.10691G>A (p.Gly3564Asp) | dbSNP gnomAD v4 |
| 4 | g.186603842C>A | CA358976777 | FAT1 | c.10684G>T (p.Gly3562Cys) c.10690G>T (p.Gly3564Cys) | dbSNP |
| 4 | g.186603842C>G | CA358976779 | FAT1 | c.10684G>C (p.Gly3562Arg) c.10690G>C (p.Gly3564Arg) | dbSNP |
| 4 | g.186603842C>T | CA358976781 | FAT1 | c.10684G>A (p.Gly3562Ser) c.10690G>A (p.Gly3564Ser) | dbSNP |
| 4 | g.186603843A= | CA1520094241 | FAT1 | c.10683T= (p.Gly3561=) c.10689T= (p.Gly3563=) | |
| 4 | g.186603843A>C | CA442889059 | FAT1 | c.10683T>G (p.Gly3561=) c.10689T>G (p.Gly3563=) | |
| 4 | g.186603843A>G | CA3165292 | FAT1 | c.10683T>C (p.Gly3561=) c.10689T>C (p.Gly3563=) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 4 | g.186603843A>T | CA442889062 | FAT1 | c.10683T>A (p.Gly3561=) c.10689T>A (p.Gly3563=) | |
| 4 | g.186603843_186603846del | CA1072009937 | FAT1 | c.10680_10683del (p.Gly3561AlafsTer17) c.10686_10689del (p.Gly3563AlafsTer17) | gnomAD v3 gnomAD v4 |
| 4 | g.186603844C>A | CA358976784 | FAT1 | c.10682G>T (p.Gly3561Val) c.10688G>T (p.Gly3563Val) | |
| 4 | g.186603844C>G | CA358976786 | FAT1 | c.10682G>C (p.Gly3561Ala) c.10688G>C (p.Gly3563Ala) | |
| 4 | g.186603844C>T | CA358976788 | FAT1 | c.10682G>A (p.Gly3561Asp) c.10688G>A (p.Gly3563Asp) | dbSNP |
| 4 | g.186603845C>A | CA358976791 | FAT1 | c.10681G>T (p.Gly3561Cys) c.10687G>T (p.Gly3563Cys) | dbSNP COSMIC COSMIC |
| 4 | g.186603845C= | CA1520094242 | FAT1 | c.10681G= (p.Gly3561=) c.10687G= (p.Gly3563=) | |
| 4 | g.186603845C>G | CA358976793 | FAT1 | c.10681G>C (p.Gly3561Arg) c.10687G>C (p.Gly3563Arg) | dbSNP |
| 4 | g.186603845C>T | CA3165293 | FAT1 | c.10681G>A (p.Gly3561Ser) c.10687G>A (p.Gly3563Ser) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 4 | g.186603846T>A | CA442889070 | FAT1 | c.10680A>T (p.Ser3560=) c.10686A>T (p.Ser3562=) | dbSNP |
| 4 | g.186603846T>C | CA442889072 | FAT1 | c.10680A>G (p.Ser3560=) c.10686A>G (p.Ser3562=) | dbSNP |
| 4 | g.186603846T>G | CA442889074 | FAT1 | c.10680A>C (p.Ser3560=) c.10686A>C (p.Ser3562=) | gnomAD v4 |
| 4 | g.186603847G>A | CA358976799 | FAT1 | c.10679C>T (p.Ser3560Leu) c.10685C>T (p.Ser3562Leu) | dbSNP gnomAD v4 |
| 4 | g.186603847G>C | CA358976797 | FAT1 | c.10679C>G (p.Ser3560Ter) c.10685C>G (p.Ser3562Ter) | dbSNP COSMIC COSMIC |
| 4 | g.186603847G>T | CA358976795 | FAT1 | c.10679C>A (p.Ser3560Ter) c.10685C>A (p.Ser3562Ter) | |
| 4 | g.186603847_186603848insTATCATTAAAAAA | CA1072009948 | FAT1 | c.10678_10679insTTTTTTAATGATA (p.Ser3560PhefsTer3) c.10684_10685insTTTTTTAATGATA (p.Ser3562PhefsTer3) | gnomAD v3 gnomAD v4 |
| 4 | g.186603848A>C | CA358976802 | FAT1 | c.10678T>G (p.Ser3560Ala) c.10684T>G (p.Ser3562Ala) | |
| 4 | g.186603848A>G | CA358976803 | FAT1 | c.10678T>C (p.Ser3560Pro) c.10684T>C (p.Ser3562Pro) | dbSNP |
| 4 | g.186603848A>T | CA358976805 | FAT1 | c.10678T>A (p.Ser3560Thr) c.10684T>A (p.Ser3562Thr) | dbSNP |
| 4 | g.186603848dup | CA645540590 | FAT1 | c.10678dup (p.Ser3560PhefsTer17) c.10684dup (p.Ser3562PhefsTer17) | COSMIC COSMIC COSMIC COSMIC |
| 4 | g.186603849G>A | CA442889082 | FAT1 | c.10677C>T (p.Tyr3559=) c.10683C>T (p.Tyr3561=) | dbSNP |
| 4 | g.186603849G>C | CA358976808 | FAT1 | c.10677C>G (p.Tyr3559Ter) c.10683C>G (p.Tyr3561Ter) | dbSNP COSMIC COSMIC |
| 4 | g.186603849G>T | CA358976810 | FAT1 | c.10677C>A (p.Tyr3559Ter) c.10683C>A (p.Tyr3561Ter) | dbSNP |
| 4 | g.186603850T>A | CA358976813 | FAT1 | c.10676A>T (p.Tyr3559Phe) c.10682A>T (p.Tyr3561Phe) | dbSNP |
| 4 | g.186603850T>C | CA358976815 | FAT1 | c.10676A>G (p.Tyr3559Cys) c.10682A>G (p.Tyr3561Cys) | dbSNP gnomAD v4 |
| 4 | g.186603850T>G | CA358976817 | FAT1 | c.10676A>C (p.Tyr3559Ser) c.10682A>C (p.Tyr3561Ser) | dbSNP |
| 4 | g.186603851A>C | CA358976820 | FAT1 | c.10675T>G (p.Tyr3559Asp) c.10681T>G (p.Tyr3561Asp) | dbSNP |
| 4 | g.186603851A>G | CA358976822 | FAT1 | c.10675T>C (p.Tyr3559His) c.10681T>C (p.Tyr3561His) | |
| 4 | g.186603851A>T | CA358976823 | FAT1 | c.10675T>A (p.Tyr3559Asn) c.10681T>A (p.Tyr3561Asn) | dbSNP |
| 4 | g.186603851_186603854delinsATTC | CA1520094243 | FAT1 | c.10672_10675delinsGAAT (p.Glu3558=) c.10678_10681delinsGAAT (p.Glu3560=) | |
| 4 | g.186603852T>A | CA358976826 | FAT1 | c.10674A>T (p.Glu3558Asp) c.10680A>T (p.Glu3560Asp) | |
| 4 | g.186603852T>C | CA442889096 | FAT1 | c.10674A>G (p.Glu3558=) c.10680A>G (p.Glu3560=) | dbSNP gnomAD v2 gnomAD v4 |
| 4 | g.186603852T>G | CA358976828 | FAT1 | c.10674A>C (p.Glu3558Asp) c.10680A>C (p.Glu3560Asp) | |
| 4 | g.186603852T= | CA1520094244 | FAT1 | c.10674A= (p.Glu3558=) c.10680A= (p.Glu3560=) | |
| 4 | g.186603856_186603858del | CA3165294 | FAT1 | c.10672_10674del (p.Glu3558del) c.10678_10680del (p.Glu3560del) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 4 | g.186603853T>A | CA358976833 | FAT1 | c.10673A>T (p.Glu3558Val) c.10679A>T (p.Glu3560Val) | dbSNP |
| 4 | g.186603853T>C | CA358976835 | FAT1 | c.10673A>G (p.Glu3558Gly) c.10679A>G (p.Glu3560Gly) | COSMIC COSMIC |
| 4 | g.186603853T>G | CA358976832 | FAT1 | c.10673A>C (p.Glu3558Ala) c.10679A>C (p.Glu3560Ala) | |
| 4 | g.186603854C>A | CA358976837 | FAT1 | c.10672G>T (p.Glu3558Ter) c.10678G>T (p.Glu3560Ter) | |
| 4 | g.186603854C= | CA1520094245 | FAT1 | c.10672G= (p.Glu3558=) c.10678G= (p.Glu3560=) | |
| 4 | g.186603854C>G | CA358976839 | FAT1 | c.10672G>C (p.Glu3558Gln) c.10678G>C (p.Glu3560Gln) | dbSNP |
| 4 | g.186603854C>T | CA358976841 | FAT1 | c.10672G>A (p.Glu3558Lys) c.10678G>A (p.Glu3560Lys) | dbSNP |
| 4 | g.186603855T>A | CA358976843 | FAT1 | c.10671A>T (p.Glu3557Asp) c.10677A>T (p.Glu3559Asp) | dbSNP |
| 4 | g.186603855T>C | CA442889109 | FAT1 | c.10671A>G (p.Glu3557=) c.10677A>G (p.Glu3559=) | dbSNP |
| 4 | g.186603855T>G | CA3165295 | FAT1 | c.10671A>C (p.Glu3557Asp) c.10677A>C (p.Glu3559Asp) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 4 | g.186603855T= | CA1520094246 | FAT1 | c.10671A= (p.Glu3557=) c.10677A= (p.Glu3559=) | |
| 4 | g.186603856T>A | CA358976847 | FAT1 | c.10670A>T (p.Glu3557Val) c.10676A>T (p.Glu3559Val) | dbSNP |
| 4 | g.186603856T>C | CA358976848 | FAT1 | c.10670A>G (p.Glu3557Gly) c.10676A>G (p.Glu3559Gly) | gnomAD v4 |
| 4 | g.186603856T>G | CA358976849 | FAT1 | c.10670A>C (p.Glu3557Ala) c.10676A>C (p.Glu3559Ala) | |
| 4 | g.186603857C>A | CA358976850 | FAT1 | c.10669G>T (p.Glu3557Ter) c.10675G>T (p.Glu3559Ter) | dbSNP |
| 4 | g.186603857C>G | CA358976851 | FAT1 | c.10669G>C (p.Glu3557Gln) c.10675G>C (p.Glu3559Gln) | dbSNP |
| 4 | g.186603857C>T | CA358976852 | FAT1 | c.10669G>A (p.Glu3557Lys) c.10675G>A (p.Glu3559Lys) | dbSNP |
| 4 | g.186603858T>A | CA442889123 | FAT1 | c.10668A>T (p.Gly3556=) c.10674A>T (p.Gly3558=) | |
| 4 | g.186603858T>C | CA442889125 | FAT1 | c.10668A>G (p.Gly3556=) c.10674A>G (p.Gly3558=) | |
| 4 | g.186603858T>G | CA442889127 | FAT1 | c.10668A>C (p.Gly3556=) c.10674A>C (p.Gly3558=) | |
| 4 | g.186603859C>A | CA358976854 | FAT1 | c.10667G>T (p.Gly3556Val) c.10673G>T (p.Gly3558Val) | dbSNP |
| 4 | g.186603859C= | CA1520094247 | FAT1 | c.10667G= (p.Gly3556=) c.10673G= (p.Gly3558=) | |
| 4 | g.186603859C>G | CA358976853 | FAT1 | c.10667G>C (p.Gly3556Ala) c.10673G>C (p.Gly3558Ala) | dbSNP gnomAD v4 |
| 4 | g.186603859C>T | CA112157408 | FAT1 | c.10667G>A (p.Gly3556Glu) c.10673G>A (p.Gly3558Glu) | dbSNP |
| 4 | g.186603860C>A | CA358976855 | FAT1 | c.10666G>T (p.Gly3556Ter) c.10672G>T (p.Gly3558Ter) | dbSNP |
| 4 | g.186603860C= | CA1520094248 | FAT1 | c.10666G= (p.Gly3556=) c.10672G= (p.Gly3558=) | |
| 4 | g.186603860C>G | CA358976856 | FAT1 | c.10666G>C (p.Gly3556Arg) c.10672G>C (p.Gly3558Arg) | dbSNP |
| 4 | g.186603860C>T | CA112157412 | FAT1 | c.10666G>A (p.Gly3556Arg) c.10672G>A (p.Gly3558Arg) | dbSNP gnomAD v4 |
| 4 | g.186603861A>C | CA442889136 | FAT1 | c.10665T>G (p.Ser3555=) c.10671T>G (p.Ser3557=) | |
| 4 | g.186603861A>G | CA442889138 | FAT1 | c.10665T>C (p.Ser3555=) c.10671T>C (p.Ser3557=) | dbSNP |
| 4 | g.186603861A>T | CA442889139 | FAT1 | c.10665T>A (p.Ser3555=) c.10671T>A (p.Ser3557=) | |
| 4 | g.186603862G>A | CA358976857 | FAT1 | c.10664C>T (p.Ser3555Phe) c.10670C>T (p.Ser3557Phe) | ClinVar dbSNP |
| 4 | g.186603862G>C | CA358976858 | FAT1 | c.10664C>G (p.Ser3555Cys) c.10670C>G (p.Ser3557Cys) | dbSNP |
| 4 | g.186603862G>T | CA358976859 | FAT1 | c.10664C>A (p.Ser3555Tyr) c.10670C>A (p.Ser3557Tyr) | |
| 4 | g.186603863A>C | CA358976860 | FAT1 | c.10663T>G (p.Ser3555Ala) c.10669T>G (p.Ser3557Ala) | |
| 4 | g.186603863A>G | CA358976861 | FAT1 | c.10663T>C (p.Ser3555Pro) c.10669T>C (p.Ser3557Pro) | |
| 4 | g.186603863A>T | CA358976862 | FAT1 | c.10663T>A (p.Ser3555Thr) c.10669T>A (p.Ser3557Thr) | |
| 4 | g.186603864A>C | CA442889155 | FAT1 | c.10662T>G (p.Ser3554=) c.10668T>G (p.Ser3556=) | |
| 4 | g.186603864A>G | CA442889153 | FAT1 | c.10662T>C (p.Ser3554=) c.10668T>C (p.Ser3556=) | |
| 4 | g.186603864A>T | CA442889149 | FAT1 | c.10662T>A (p.Ser3554=) c.10668T>A (p.Ser3556=) | |
| 4 | g.186603865G>A | CA3165296 | FAT1 | c.10661C>T (p.Ser3554Phe) c.10667C>T (p.Ser3556Phe) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 4 | g.186603865G>C | CA358976863 | FAT1 | c.10661C>G (p.Ser3554Cys) c.10667C>G (p.Ser3556Cys) | |
| 4 | g.186603865G= | CA1520094249 | FAT1 | c.10661C= (p.Ser3554=) c.10667C= (p.Ser3556=) | |
| 4 | g.186603865G>T | CA358976864 | FAT1 | c.10661C>A (p.Ser3554Tyr) c.10667C>A (p.Ser3556Tyr) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 4 | g.186603866A= | CA1520094250 | FAT1 | c.10660T= (p.Ser3554=) c.10666T= (p.Ser3556=) | |
| 4 | g.186603866A>C | CA3165297 | FAT1 | c.10660T>G (p.Ser3554Ala) c.10666T>G (p.Ser3556Ala) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 4 | g.186603866A>G | CA358976865 | FAT1 | c.10660T>C (p.Ser3554Pro) c.10666T>C (p.Ser3556Pro) | |
| 4 | g.186603866A>T | CA3165298 | FAT1 | c.10660T>A (p.Ser3554Thr) c.10666T>A (p.Ser3556Thr) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 4 | g.186603866_186603867delinsCA | CA2580071728 | FAT1 | c.10659_10660delinsTG (p.Ser3554Ala) c.10665_10666delinsTG (p.Ser3556Ala) | ClinVar |
| 4 | g.186603867G>A | CA3165299 | FAT1 | c.10659C>T (p.Thr3553=) c.10665C>T (p.Thr3555=) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 4 | g.186603867G>C | CA442889162 | FAT1 | c.10659C>G (p.Thr3553=) c.10665C>G (p.Thr3555=) | |
| 4 | g.186603867G= | CA1520094251 | FAT1 | c.10659C= (p.Thr3553=) c.10665C= (p.Thr3555=) | |
| 4 | g.186603867G>T | CA442889160 | FAT1 | c.10659C>A (p.Thr3553=) c.10665C>A (p.Thr3555=) | |
| 4 | g.186603868G>A | CA358976866 | FAT1 | c.10658C>T (p.Thr3553Ile) c.10664C>T (p.Thr3555Ile) | |
| 4 | g.186603868G>C | CA358976867 | FAT1 | c.10658C>G (p.Thr3553Ser) c.10664C>G (p.Thr3555Ser) | dbSNP |
| 4 | g.186603868G>T | CA358976868 | FAT1 | c.10658C>A (p.Thr3553Asn) c.10664C>A (p.Thr3555Asn) | COSMIC |
| 4 | g.186603869T>A | CA358976869 | FAT1 | c.10657A>T (p.Thr3553Ser) c.10663A>T (p.Thr3555Ser) | dbSNP |
| 4 | g.186603869T>C | CA358976870 | FAT1 | c.10657A>G (p.Thr3553Ala) c.10663A>G (p.Thr3555Ala) | dbSNP |
| 4 | g.186603869T>G | CA358976871 | FAT1 | c.10657A>C (p.Thr3553Pro) c.10663A>C (p.Thr3555Pro) | dbSNP |
| 4 | g.186603870G>A | CA442889173 | FAT1 | c.10656C>T (p.Ile3552=) c.10662C>T (p.Ile3554=) | dbSNP |
| 4 | g.186603870G>C | CA3165300 | FAT1 | c.10656C>G (p.Ile3552Met) c.10662C>G (p.Ile3554Met) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 4 | g.186603870G= | CA1520094252 | FAT1 | c.10656C= (p.Ile3552=) c.10662C= (p.Ile3554=) | |
| 4 | g.186603870G>T | CA442889181 | FAT1 | c.10656C>A (p.Ile3552=) c.10662C>A (p.Ile3554=) | dbSNP |
| 4 | g.186603871A>C | CA358976872 | FAT1 | c.10655T>G (p.Ile3552Ser) c.10661T>G (p.Ile3554Ser) | |
| 4 | g.186603871A>G | CA358976874 | FAT1 | c.10655T>C (p.Ile3552Thr) c.10661T>C (p.Ile3554Thr) | dbSNP |
| 4 | g.186603871A>T | CA358976873 | FAT1 | c.10655T>A (p.Ile3552Asn) c.10661T>A (p.Ile3554Asn) | dbSNP |
| 4 | g.186603872T>A | CA358976875 | FAT1 | c.10654A>T (p.Ile3552Phe) c.10660A>T (p.Ile3554Phe) | dbSNP |
| 4 | g.186603872T>C | CA358976876 | FAT1 | c.10654A>G (p.Ile3552Val) c.10660A>G (p.Ile3554Val) | dbSNP |
| 4 | g.186603872T>G | CA358976877 | FAT1 | c.10654A>C (p.Ile3552Leu) c.10660A>C (p.Ile3554Leu) | dbSNP gnomAD v2 gnomAD v4 |
| 4 | g.186603872T= | CA1520094253 | FAT1 | c.10654A= (p.Ile3552=) c.10660A= (p.Ile3554=) | |
| 4 | g.186603873G>A | CA442889192 | FAT1 | c.10653C>T (p.Phe3551=) c.10659C>T (p.Phe3553=) | gnomAD v4 |
| 4 | g.186603873G>C | CA358976879 | FAT1 | c.10653C>G (p.Phe3551Leu) c.10659C>G (p.Phe3553Leu) | dbSNP |
| 4 | g.186603873G>T | CA358976880 | FAT1 | c.10653C>A (p.Phe3551Leu) c.10659C>A (p.Phe3553Leu) |