![]()
Description of the mutations of BRAF (NM_004333) Mutants
![]()
Keys for Mutation Description
A.A. substitution
Truncation
NT deletion
NT insertion
Truncation
NT deletion
NT insertion
R280G: Arg at aa-position 280 mutated to Gly
R342X: R at aa-position 342 mutated to a stop codon and caused truncation of the protein
N268_D2: The deletion starts at nt#268. Two bases (including nt268) are deleted
N478-I6: The insertion starts after nt#478. Six bases are inserted
R342X: R at aa-position 342 mutated to a stop codon and caused truncation of the protein
N268_D2: The deletion starts at nt#268. Two bases (including nt268) are deleted
N478-I6: The insertion starts after nt#478. Six bases are inserted
| SKU | Mutation Description | Affected Codon# | Affected NT# | Description | Effect | Affected Protein Domain |
| RC400154 | V600A | 600 | c.1799 | T>C | missense | kinase |
| RC400155 | V600E | 600 | c.1799 | T>A | missense | kinase |
| RC400156 | V600G | 600 | c.1799 | T>G | missense | kinase |
| RC400157 | V600M | 600 | c.1798 | G>A | missense | kinase |
| RC400158 | V600D | 600 | c.1799_1800 | TG>AT | missense | kinase |
| RC400159 | V600R | 600 | c.1798_1799 | GT>AG | missense | kinase |
| RC400160 | V600K | 600 | c.1798_1799 | GT>AA | missense | kinase |
| RC400321 | L597Q | 597 | c.1790 | T>A | Missense | |
| RC400322 | L597V | 597 | c.1789 | C>G | Missense | |
| RC400323 | G469E | 469 | c.1406 | G>A | Missense | |
| RC400324 | G469A | 469 | c.1406 | G>C | Missense | |
| RC400325 | K601E | 601 | c.1801 | A>G | Missense | |
| RC400326 | G466V | 466 | c.1397 | G>T | Missense | |
| RC400327 | Y472S | 472 | c.1415 | A>C | Missense | |
| RC400328 | G464V | 464 | c.1391 | G>T | Missense | |
| RC402700 | T241P | 241 | 721 | A>C | Costello syndrome | |
| RC402701 | T244P | 244 | 730 | A>C | Cardio-facio-cutaneous syndrome | |
| RC402702 | A246P | 246 | 736 | G>C | Cardio-facio-cutaneous syndrome | |
| RC402703 | Q257R | 257 | 770 | A>G | Cardio-facio-cutaneous syndrome | |
| RC402704 | Q257K | 257 | 769 | C>A | Cardio-facio-cutaneous syndrome | |
| RC402705 | Q262R | 262 | 785 | A>G | Cardio-facio-cutaneous syndrome | |
| RC402706 | Q262K | 262 | 784 | C>A | Cardio-facio-cutaneous syndrome | |
| RC402707 | G464R | 464 | 1390 | G>C | Cardio-facio-cutaneous syndrome | |
| RC402708 | S467A | 467 | 1399 | T>G | Cardio-facio-cutaneous syndrome | |
| RC402709 | F468S | 468 | 1403 | T>C | Cardio-facio-cutaneous syndrome | |
| RC402710 | L485F | 485 | 1455 | G>C | Cardio-facio-cutaneous syndrome | |
| RC402711 | L485S | 485 | 1454 | T>C | Cardio-facio-cutaneous syndrome | |
| RC402712 | v487G | 487 | 1460 | T>G | Cardio-facio-cutaneous syndrome | |
| RC402713 | K499N | 499 | 1497 | A>C | Cardio-facio-cutaneous syndrome | |
| RC402714 | K499E | 499 | 1495 | A>G | Cardio-facio-cutaneous syndrome | |
| RC402715 | E501G | 501 | 1502 | A>G | Cardio-facio-cutaneous syndrome | |
| RC402716 | E501v | 501 | 1502 | A>T | Cardio-facio-cutaneous syndrome | |
| RC402717 | E501K | 501 | 1501 | G>A | Cardio-facio-cutaneous syndrome | |
| RC402718 | L525P | 525 | 1574 | T>C | Cardio-facio-cutaneous syndrome | |
| RC402719 | G534R | 534 | 1600 | G>C | Cardio-facio-cutaneous syndrome | |
| RC402720 | D565E | 565 | 1695 | T>G | Cardio-facio-cutaneous syndrome | |
| RC402721 | N580D | 580 | 1738 | A>G | Cardio-facio-cutaneous syndrome | |
| RC402722 | N581D | 581 | 1741 | A>G | Cardio-facio-cutaneous syndrome | |
| RC402723 | F595L | 595 | 1785 | T>G | Cardio-facio-cutaneous syndrome | |
| RC402724 | F595L | 595 | 1785 | T>A | Cardio-facio-cutaneous syndrome | |
| RC402725 | G596v | 596 | 1787 | G>T | Cardio-facio-cutaneous syndrome | |
| RC402726 | T599R | 599 | 1796 | C>G | Cardio-facio-cutaneous syndrome | |
| RC402727 | D638E | 638 | 1914 | T>A | Cardio-facio-cutaneous syndrome |


