Variant (rsID / SNP)

rs114447625

rs114447625 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CATSPER3. Location: chromosome 5, position 134,332,143. The table records no clinical significance for this variant.

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Reference-table entries

CATSPER3Not classified

Variant type: missense_variant
Chromosome / position: 5:134332143
HGVS: NM_178019.3,c.433G>A,p.Ala145Thr
Allele change: Missense_A145T

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.