Variant (rsID / SNP)
rs140504
rs140504 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to BCR. Location: chromosome 22, position 23,627,369. The table records no clinical significance for this variant.
Reference-table entries
BCRNot classified
- Variant type
- missense_variant
- Chromosome / position
- 22:23627369
- HGVS
- NM_004327.4,c.2387A>G,p.Asn796Ser
- Allele change
- Missense_N796S
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.