Variant (rsID / SNP)

rs121913528

rs121913528 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to KRAS. Location: chromosome 12, position 25,380,283. 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: 12:25380283
Cytoband: 12p12.1
HGVS: NM_033360.4(KRAS):c.175G>A (p.Ala59Thr)
Allele change: Missense_A59T

Associated conditions / phenotypes

Bladder cancer, transitional cell, somatic|Neoplasm of the large intestine

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.