Variant (rsID / SNP)

rs397517144

rs397517144 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to HRAS. Location: chromosome 11, position 532,686. Clinical significance in the table: Benign.

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Reference-table entries

HRASBenign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 11:532686
Cytoband: 11p15.5
HGVS: NM_005343.4(HRAS):c.520C>T (p.Pro174Ser)
Allele change: Silent

Associated conditions / phenotypes

Costello syndrome|RASopathy|6 conditions|Hereditary cancer-predisposing 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.