Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs1156783831
- Species
- Homo sapiens
- Symbol
- rs1156783831
- Category
- Variant
- Variant type
- SNP
- Overlaps
- TRIM37
- Location
- 17:59012345
- Nucleotide Change
- G>A
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- NC_000017.11:g.59012345G>A
- HGVS.c name
- ENSEMBL:ENST00000262294.12:c.2678C>T
- ENSEMBL:ENST00000393065.6:c.2576C>T
- HGVS.p name
- ENSP00000262294:p.Ser893Leu
- ENSP00000376784:p.Ser859Leu
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr17:58967201...59106921 (139.72 kb)
- Assembly version
- Not Available
- Viewer Help
Data currently unavailable; sequence viewer under construction