Variant (rsID / SNP)

rs141439443

rs141439443 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CENPF. Location: chromosome 1, position 214,832,346. Clinical significance in the table: Uncertain significance.

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Reference-table entries

CENPFUncertain significance

Clinical significance (as recorded): Uncertain significance
Variant type: single nucleotide variant
Chromosome / position: 1:214832346
Cytoband: 1q41
HGVS: NM_016343.4(CENPF):c.9116C>G (p.Thr3039Arg)
Allele change: Missense_T3039R

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.