Variant (rsID / SNP)

rs180177038

rs180177038 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to BRAF. Location: chromosome 7, position 140,477,807. Clinical significance in the table: Pathogenic/Likely pathogenic.

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Reference-table entries

BRAFPathogenic

Clinical significance (as recorded): Pathogenic/Likely pathogenic
Variant type: single nucleotide variant
Chromosome / position: 7:140477807
Cytoband: 7q34
HGVS: NM_004333.6(BRAF):c.1501G>A (p.Glu501Lys)
Allele change: Missense_E501K

Associated conditions / phenotypes

Cardiofaciocutaneous syndrome 1|RASopathy|Noonan syndrome|Cardio-facio-cutaneous syndrome

Public references

dbSNP
ClinVar
Ensembl
gnomAD

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.