Genetics University — Research, Education, Medical Genetics
Knowledge Hub

Variant (rsID / SNP)

rs201004111

APC

rs201004111 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to APC. Location: chromosome 5, position 112,174,770. Clinical significance in the table: Conflicting interpretations of pathogenicity.

ShareE-MailWhatsAppLinkedInXFacebookTelegram

Reference-table entries

APCConflicting interpretations
Clinical significance (as recorded)
Conflicting interpretations of pathogenicity
Variant type
single nucleotide variant
Chromosome / position
5:112174770
Cytoband
5q22.2
HGVS
NM_000038.6(APC):c.3479C>A (p.Thr1160Lys)
Allele change
Missense_T1160K

Associated conditions / phenotypes

Hereditary cancer-predisposing syndrome|Colorectal adenoma|Familial adenomatous polyposis 1|Familial adenomatous polyposis 1

Public references

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