Variant (rsID / SNP)

rs140079

rs140079 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PRR14L. Location: chromosome 22, position 32,110,943. The table records no clinical significance for this variant.

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Reference-table entries

PRR14LNot classified

Variant type: missense_variant
Chromosome / position: 22:32110943
HGVS: NM_173566.3,c.2882C>T,p.Thr961Ile
Allele change: Missense_T961I

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.