Variant (rsID / SNP)

rs114717799

rs114717799 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CENPF. Location: chromosome 1, position 214,815,304. Clinical significance in the table: Benign.

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Reference-table entries

CENPFBenign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 1:214815304
Cytoband: 1q41
HGVS: NM_016343.4(CENPF):c.3623C>T (p.Ala1208Val)
Allele change: Missense_A1208V

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.