Variant (rsID / SNP)

rs1256149

rs1256149 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to AKAP5, ZBTB25. Location: chromosome 14, position 64,935,720. The table records no clinical significance for this variant.

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Reference-table entries

AKAP5Not classified

Variant type: missense_variant
Chromosome / position: 14:64935720
HGVS: NM_004857.3,c.608C>T,p.Thr203Ile
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.