Project HERA

BRAF variants

Every BRAF variant the pipeline has interpreted, classified against the ClinGen expert-panel specification for the gene where one exists.

26 variants

BRAF variants

Newest first. Each row opens the full report, criterion by criterion.

26 shown

Variant

Protein change

Classification

BRAF NM_004333.5:c.2107G>A

NP_004324.2:p.(E703K)

BRAF NM_004333.5:c.1447A>G

NP_004324.2:p.(K483E)

BRAF NM_004333.6:c.1741A>T

NP_004324.2:p.(N581Y)

BRAF NM_004333.5:c.1661T>C

NP_004324.2:p.(I554T)

BRAF NM_004333.5:c.1330C>T

NP_004324.2:p.(R444W)

BRAF NM_001354609.1:c.1068A>G

NP_001341538.1:p.(Q356=)

BRAF NM_001354609.1:c.736G>C

NP_001341538.1:p.(A246P)

Likely Pathogenic

BRAF NM_001354609.1:c.739T>G

NP_001341538.1:p.(F247V)

Likely Pathogenic

BRAF NM_001354609.1:c.1406G>A

NP_001341538.1:p.(G469E)

BRAF NM_001354609.1:c.739T>C

NP_001341538.1:p.(F247L)

BRAF NM_001354609.1:c.1799T>G

NP_001341538.1:p.(V600G)

Likely Pathogenic

BRAF NM_001354609.1:c.1929A>G

NP_001341538.1:p.(G643=)

BRAF NM_001354609.1:c.1024A>G

NP_001341538.1:p.(I342V)

BRAF NM_001354609.1:c.1383A>G

NP_001341538.1:p.(Q461=)

BRAF NM_001354609.1:c.722C>A

NP_001341538.1:p.(T241K)

Likely Pathogenic

BRAF NM_001354609.1:c.741T>G

NP_001341538.1:p.(F247L)

Likely Pathogenic

BRAF NM_001354609.1:c.2127+3A>G

NP_001341538.1:p.?

BRAF NM_001354609.1:c.708C>T

NP_001341538.1:p.(N236=)

BRAF NM_001354609.1:c.622A>G

NP_001341538.1:p.(I208V)

BRAF NM_001354609.1:c.793G>C

NP_001341538.1:p.(G265R)

BRAF NM_001354609.1:c.1787G>T

NP_001341538.1:p.(G596V)

BRAF NM_001354609.1:c.730A>C

NP_001341538.1:p.(T244P)

BRAF NM_001354609.1:c.483G>C

NP_001341538.1:p.(L161=)

BRAF NM_001354609.1:c.1595G>A

NP_001341538.1:p.(C532Y)

BRAF NM_001354609.1:c.1796C>G

NP_001341538.1:p.(T599R)

BRAF NM_001354609.1:c.770A>G

NP_001341538.1:p.(Q257R)