Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs1461316661
- Species
- Homo sapiens
- Symbol
- rs1461316661
- Category
- Variant
- Variant type
- SNP
- Overlaps
- BTBD7
- Location
- 14:93242812
- Nucleotide Change
- T>C
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- NC_000014.9:g.93242812T>C
- HGVS.c name
- ENSEMBL:ENST00000334746.10:c.2860A>G
- ENSEMBL:ENST00000355125.3:n.1560A>G
- HGVS.p name
- ENSP00000335615:p.Arg954Gly
- ENSP00000450778:p.Arg569Gly
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr14:93237550...93333092 (95.54 kb)
- Assembly version
- Not Available
- Viewer Help
Data currently unavailable; sequence viewer under construction