Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs1044281127
- Species
- Homo sapiens
- Symbol
- rs1044281127
- Category
- Variant
- Variant type
- SNP
- Overlaps
- RUFY2
- Location
- 10:68383841
- Nucleotide Change
- T>C
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- NC_000010.11:g.68383841T>C
- HGVS.c name
- ENSEMBL:ENST00000388768.6:c.1001A>G
- ENSEMBL:ENST00000399200.7:c.794A>G
- HGVS.p name
- ENSP00000373420:p.Asn334Ser
- ENSP00000382151:p.Asn265Ser
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr10:68341107...68407294 (66.19 kb)
- Assembly version
- Not Available
- Viewer Help
Data currently unavailable; sequence viewer under construction