Variant (rsID / SNP)

rs114152031

rs114152031 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to AKT3. Location: chromosome 1, position 243,827,863. Clinical significance in the table: Likely benign.

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Reference-table entries

AKT3Likely benign

Clinical significance (as recorded): Likely benign
Variant type: single nucleotide variant
Chromosome / position: 1:243827863
Cytoband: 1q44
HGVS: NM_005465.7(AKT3):c.284+211T>C
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.