Genetics University — Research, Education, Medical Genetics
Knowledge Hub

Variant (rsID / SNP)

rs2602141

TP53BP1

rs2602141 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TP53BP1. Location: chromosome 15, position 43,724,646. The table records no clinical significance for this variant.

ShareE-MailWhatsAppLinkedInXFacebookTelegram

Reference-table entries

TP53BP1Not classified
Variant type
missense_variant
Chromosome / position
15:43724646
HGVS
NM_001141980.3,c.3421A>C,p.Lys1141Gln
Allele change
Missense_K1141Q

Public references

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