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Variant (rsID / SNP)

rs193929331

KRAS

rs193929331 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to KRAS. Location: chromosome 12, position 25,398,306. Clinical significance in the table: Pathogenic/Likely pathogenic.

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Reference-table entries

KRASPathogenic
Clinical significance (as recorded)
Pathogenic/Likely pathogenic
Variant type
single nucleotide variant
Chromosome / position
12:25398306
Cytoband
12p12.1
HGVS
NM_004985.5(KRAS):c.13A>G (p.Lys5Glu)
Allele change
Missense_K5E

Associated conditions / phenotypes

Noonan syndrome 3|RASopathy|Noonan syndrome|Prostate cancer, hereditary, 1

Public references

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