Variant (rsID / SNP)

rs11601431

rs11601431 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TP53AIP1. Location: chromosome 11, position 128,805,548. The table records no clinical significance for this variant.

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Reference-table entries

TP53AIP1Not classified

Variant type: missense_variant
Chromosome / position: 11:128805548
HGVS: NM_022112.3,c.313C>T,p.Pro105Ser
Allele change: Silent

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.