Variant (rsID / SNP)

rs34960436

rs34960436 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CCDC198. Location: chromosome 14, position 57,947,421. Clinical significance in the table: Benign.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

CCDC198Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 14:57947421
Cytoband: 14q22.3
HGVS: NM_018168.4(CCDC198):c.547C>T (p.Gln183Ter)
Allele change: Nonsense_Q183X

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.