Unique variants in the BRAF gene

Information The variants shown are described using the NM_004333.5 transcript reference sequence.

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Effect     

Reported     

Exon     

AscendingDNA change (cDNA)     

Published as     

RNA change     

Protein     

GVS function     

Clinical classification     

DNA change (genomic) (hg38)     

Published as     

Reference     

DB-ID     

dbSNP ID     

Frequency     

Variant remarks     

Owner     
+/. 3 15 c.1799T>A - r.(?) p.(Val600Glu) - Pathogenic, ClinVar g.176429T>A, g.140753336A>T V600E A A Mohamed Yusoff et al.(2021), dbSNP, (OMIM 0001), dbSNP, ClinVar, 1 more item BRAF_000001 rs113488022 11/50, 1 BRAF V600E Nur Aisyah Athirah, Nuur Athirah Binti Mohd Daud
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