Variant (rsID / SNP)
rs3128658
rs3128658 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to DNAH14. Location: chromosome 1, position 225,273,248. Clinical significance in the table: Benign.
Reference-table entries
DNAH14Benign
- Clinical significance (as recorded)
- Benign
- Variant type
- single nucleotide variant
- Chromosome / position
- 1:225273248
- Cytoband
- 1q42.12
- HGVS
- NM_001367479.1(DNAH14):c.3330G>T (p.Met1110Ile)
- Allele change
- Missense_M1110I
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.