| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 4 | g.125468697G>A | CA358128444 | FAT4 | c.12091G>A (p.Glu4031Lys) c.6862G>A (p.Glu2288Lys) c.6874G>A (p.Glu2292Lys) c.12085G>A (p.Glu4029Lys) | ClinVar dbSNP |
| 4 | g.125468697G>C | CA358128447 | FAT4 | c.12091G>C (p.Glu4031Gln) c.6862G>C (p.Glu2288Gln) c.6874G>C (p.Glu2292Gln) c.12085G>C (p.Glu4029Gln) | |
| 4 | g.125468697G= | CA1491662364 | FAT4 | c.12091G= (p.Glu4031=) c.6862G= (p.Glu2288=) c.6874G= (p.Glu2292=) c.12085G= (p.Glu4029=) | |
| 4 | g.125468697G>T | CA358128449 | FAT4 | c.12091G>T (p.Glu4031Ter) c.6862G>T (p.Glu2288Ter) c.6874G>T (p.Glu2292Ter) c.12085G>T (p.Glu4029Ter) | |
| 4 | g.125468698A>C | CA358128461 | FAT4 | c.12092A>C (p.Glu4031Ala) c.6863A>C (p.Glu2288Ala) c.6875A>C (p.Glu2292Ala) c.12086A>C (p.Glu4029Ala) | |
| 4 | g.125468698A>G | CA358128452 | FAT4 | c.12092A>G (p.Glu4031Gly) c.6863A>G (p.Glu2288Gly) c.6875A>G (p.Glu2292Gly) c.12086A>G (p.Glu4029Gly) | |
| 4 | g.125468698A>T | CA358128455 | FAT4 | c.12092A>T (p.Glu4031Val) c.6863A>T (p.Glu2288Val) c.6875A>T (p.Glu2292Val) c.12086A>T (p.Glu4029Val) | |
| 4 | g.125468699A>C | CA358128463 | FAT4 | c.12093A>C (p.Glu4031Asp) c.6864A>C (p.Glu2288Asp) c.6876A>C (p.Glu2292Asp) c.12087A>C (p.Glu4029Asp) | |
| 4 | g.125468699A>G | CA441372989 | FAT4 | c.12093A>G (p.Glu4031=) c.6864A>G (p.Glu2288=) c.6876A>G (p.Glu2292=) c.12087A>G (p.Glu4029=) | |
| 4 | g.125468699A>T | CA358128465 | FAT4 | c.12093A>T (p.Glu4031Asp) c.6864A>T (p.Glu2288Asp) c.6876A>T (p.Glu2292Asp) c.12087A>T (p.Glu4029Asp) | ClinVar dbSNP |
| 4 | g.125468700A>C | CA358128468 | FAT4 | c.12094A>C (p.Ile4032Leu) c.6865A>C (p.Ile2289Leu) c.6877A>C (p.Ile2293Leu) c.12088A>C (p.Ile4030Leu) | |
| 4 | g.125468700A>G | CA358128471 | FAT4 | c.12094A>G (p.Ile4032Val) c.6865A>G (p.Ile2289Val) c.6877A>G (p.Ile2293Val) c.12088A>G (p.Ile4030Val) | |
| 4 | g.125468700A>T | CA358128473 | FAT4 | c.12094A>T (p.Ile4032Phe) c.6865A>T (p.Ile2289Phe) c.6877A>T (p.Ile2293Phe) c.12088A>T (p.Ile4030Phe) | |
| 4 | g.125468701T>A | CA358128475 | FAT4 | c.12095T>A (p.Ile4032Asn) c.6866T>A (p.Ile2289Asn) c.6878T>A (p.Ile2293Asn) c.12089T>A (p.Ile4030Asn) | |
| 4 | g.125468701T>C | CA358128481 | FAT4 | c.12095T>C (p.Ile4032Thr) c.6866T>C (p.Ile2289Thr) c.6878T>C (p.Ile2293Thr) c.12089T>C (p.Ile4030Thr) | |
| 4 | g.125468701T>G | CA358128478 | FAT4 | c.12095T>G (p.Ile4032Ser) c.6866T>G (p.Ile2289Ser) c.6878T>G (p.Ile2293Ser) c.12089T>G (p.Ile4030Ser) | |
| 4 | g.125468702T>A | CA441372990 | FAT4 | c.12096T>A (p.Ile4032=) c.6867T>A (p.Ile2289=) c.6879T>A (p.Ile2293=) c.12090T>A (p.Ile4030=) | |
| 4 | g.125468702T>C | CA441372991 | FAT4 | c.12096T>C (p.Ile4032=) c.6867T>C (p.Ile2289=) c.6879T>C (p.Ile2293=) c.12090T>C (p.Ile4030=) | |
| 4 | g.125468702T>G | CA358128486 | FAT4 | c.12096T>G (p.Ile4032Met) c.6867T>G (p.Ile2289Met) c.6879T>G (p.Ile2293Met) c.12090T>G (p.Ile4030Met) | |
| 4 | g.125468703G>A | CA358128487 | FAT4 | c.12097G>A (p.Ala4033Thr) c.6868G>A (p.Ala2290Thr) c.6880G>A (p.Ala2294Thr) c.12091G>A (p.Ala4031Thr) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
| 4 | g.125468703G>C | CA358128490 | FAT4 | c.12097G>C (p.Ala4033Pro) c.6868G>C (p.Ala2290Pro) c.6880G>C (p.Ala2294Pro) c.12091G>C (p.Ala4031Pro) | |
| 4 | g.125468703G= | CA1491662365 | FAT4 | c.12097G= (p.Ala4033=) c.6868G= (p.Ala2290=) c.6880G= (p.Ala2294=) c.12091G= (p.Ala4031=) | |
| 4 | g.125468703G>T | CA358128492 | FAT4 | c.12097G>T (p.Ala4033Ser) c.6868G>T (p.Ala2290Ser) c.6880G>T (p.Ala2294Ser) c.12091G>T (p.Ala4031Ser) | |
| 4 | g.125468704C>A | CA358128495 | FAT4 | c.12098C>A (p.Ala4033Asp) c.6869C>A (p.Ala2290Asp) c.6881C>A (p.Ala2294Asp) c.12092C>A (p.Ala4031Asp) | |
| 4 | g.125468704C>G | CA358128496 | FAT4 | c.12098C>G (p.Ala4033Gly) c.6869C>G (p.Ala2290Gly) c.6881C>G (p.Ala2294Gly) c.12092C>G (p.Ala4031Gly) | |
| 4 | g.125468704C>T | CA358128500 | FAT4 | c.12098C>T (p.Ala4033Val) c.6869C>T (p.Ala2290Val) c.6881C>T (p.Ala2294Val) c.12092C>T (p.Ala4031Val) | COSMIC COSMIC |
| 4 | g.125468705C>A | CA104860407 | FAT4 | c.12099C>A (p.Ala4033=) c.6870C>A (p.Ala2290=) c.6882C>A (p.Ala2294=) c.12093C>A (p.Ala4031=) | ClinVar dbSNP |
| 4 | g.125468705C= | CA1491662366 | FAT4 | c.12099C= (p.Ala4033=) c.6870C= (p.Ala2290=) c.6882C= (p.Ala2294=) c.12093C= (p.Ala4031=) | |
| 4 | g.125468705C>G | CA441372992 | FAT4 | c.12099C>G (p.Ala4033=) c.6870C>G (p.Ala2290=) c.6882C>G (p.Ala2294=) c.12093C>G (p.Ala4031=) | |
| 4 | g.125468705C>T | CA3074010 | FAT4 | c.12099C>T (p.Ala4033=) c.6870C>T (p.Ala2290=) c.6882C>T (p.Ala2294=) c.12093C>T (p.Ala4031=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC COSMIC |
| 4 | g.125468706G>A | CA358128505 | FAT4 | c.12100G>A (p.Glu4034Lys) c.6871G>A (p.Glu2291Lys) c.6883G>A (p.Glu2295Lys) c.12094G>A (p.Glu4032Lys) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 COSMIC COSMIC |
| 4 | g.125468706G>C | CA358128506 | FAT4 | c.12100G>C (p.Glu4034Gln) c.6871G>C (p.Glu2291Gln) c.6883G>C (p.Glu2295Gln) c.12094G>C (p.Glu4032Gln) | |
| 4 | g.125468706G= | CA1491662367 | FAT4 | c.12100G= (p.Glu4034=) c.6871G= (p.Glu2291=) c.6883G= (p.Glu2295=) c.12094G= (p.Glu4032=) | |
| 4 | g.125468706G>T | CA358128510 | FAT4 | c.12100G>T (p.Glu4034Ter) c.6871G>T (p.Glu2291Ter) c.6883G>T (p.Glu2295Ter) c.12094G>T (p.Glu4032Ter) | |
| 4 | g.125468707A>C | CA358128512 | FAT4 | c.12101A>C (p.Glu4034Ala) c.6872A>C (p.Glu2291Ala) c.6884A>C (p.Glu2295Ala) c.12095A>C (p.Glu4032Ala) | |
| 4 | g.125468707A>G | CA358128517 | FAT4 | c.12101A>G (p.Glu4034Gly) c.6872A>G (p.Glu2291Gly) c.6884A>G (p.Glu2295Gly) c.12095A>G (p.Glu4032Gly) | |
| 4 | g.125468707A>T | CA358128515 | FAT4 | c.12101A>T (p.Glu4034Val) c.6872A>T (p.Glu2291Val) c.6884A>T (p.Glu2295Val) c.12095A>T (p.Glu4032Val) | |
| 4 | g.125468711_125468714del | CA2672011535 | FAT4 | c.12105_12108del (p.Glu4035AspfsTer2) c.6876_6879del (p.Glu2292AspfsTer2) c.6888_6891del (p.Glu2296AspfsTer2) c.12099_12102del (p.Glu4033AspfsTer2) | gnomAD v4 |
| 4 | g.125468708A>C | CA358128520 | FAT4 | c.12102A>C (p.Glu4034Asp) c.6873A>C (p.Glu2291Asp) c.6885A>C (p.Glu2295Asp) c.12096A>C (p.Glu4032Asp) | |
| 4 | g.125468708A>G | CA441372993 | FAT4 | c.12102A>G (p.Glu4034=) c.6873A>G (p.Glu2291=) c.6885A>G (p.Glu2295=) c.12096A>G (p.Glu4032=) | |
| 4 | g.125468708A>T | CA358128521 | FAT4 | c.12102A>T (p.Glu4034Asp) c.6873A>T (p.Glu2291Asp) c.6885A>T (p.Glu2295Asp) c.12096A>T (p.Glu4032Asp) | |
| 4 | g.125468709G>A | CA358128525 | FAT4 | c.12103G>A (p.Glu4035Lys) c.6874G>A (p.Glu2292Lys) c.6886G>A (p.Glu2296Lys) c.12097G>A (p.Glu4033Lys) | |
| 4 | g.125468709G>C | CA358128532 | FAT4 | c.12103G>C (p.Glu4035Gln) c.6874G>C (p.Glu2292Gln) c.6886G>C (p.Glu2296Gln) c.12097G>C (p.Glu4033Gln) | gnomAD v4 |
| 4 | g.125468709G>T | CA358128530 | FAT4 | c.12103G>T (p.Glu4035Ter) c.6874G>T (p.Glu2292Ter) c.6886G>T (p.Glu2296Ter) c.12097G>T (p.Glu4033Ter) | COSMIC COSMIC |
| 4 | g.125468710A>C | CA358128534 | FAT4 | c.12104A>C (p.Glu4035Ala) c.6875A>C (p.Glu2292Ala) c.6887A>C (p.Glu2296Ala) c.12098A>C (p.Glu4033Ala) | |
| 4 | g.125468710A>G | CA358128535 | FAT4 | c.12104A>G (p.Glu4035Gly) c.6875A>G (p.Glu2292Gly) c.6887A>G (p.Glu2296Gly) c.12098A>G (p.Glu4033Gly) | |
| 4 | g.125468710A>T | CA358128538 | FAT4 | c.12104A>T (p.Glu4035Val) c.6875A>T (p.Glu2292Val) c.6887A>T (p.Glu2296Val) c.12098A>T (p.Glu4033Val) | |
| 4 | g.125468711A>C | CA358128542 | FAT4 | c.12105A>C (p.Glu4035Asp) c.6876A>C (p.Glu2292Asp) c.6888A>C (p.Glu2296Asp) c.12099A>C (p.Glu4033Asp) | |
| 4 | g.125468711A>G | CA441372994 | FAT4 | c.12105A>G (p.Glu4035=) c.6876A>G (p.Glu2292=) c.6888A>G (p.Glu2296=) c.12099A>G (p.Glu4033=) | |
| 4 | g.125468711A>T | CA358128543 | FAT4 | c.12105A>T (p.Glu4035Asp) c.6876A>T (p.Glu2292Asp) c.6888A>T (p.Glu2296Asp) c.12099A>T (p.Glu4033Asp) |