Variant ID: 7-140453136-A-T

NM_004333.4(BRAF):c.1799T>A;(p.Val600Glu)

This variant was identified in 10528 publications



Variant-Specific Resource Links:
gnomAD v2.1.1
Mutalizer Name Checker
Google
UCSC Genome Browser
ClinVar

Publications:

Alternative transcript annotations:

Transcript cDNA Protein Consequence Exon Intron
ENST00000288602.6 c.1799T>A p.Val600Glu missense_variant 15/18 -
ENST00000479537.1 c.83T>A p.Val28Glu missense_variant,NMD_transcript_variant 2/6 -
ENST00000496384.2 c.623T>A p.Val208Glu missense_variant 6/10 -
ENST00000497784.1 c.*1249T>A - 3_prime_UTR_variant,NMD_transcript_variant 16/19 -
NM_001354609.2 c.1799T>A p.Val600Glu missense_variant 15/19 -
NM_004333.6 c.1799T>A p.Val600Glu missense_variant 15/18 -
NR_148928.2 n.2898T>A - non_coding_transcript_exon_variant 15/18 -