Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs756391768
- Species
- Homo sapiens
- Symbol
- rs756391768
- Category
- Variant
- Variant type
- SNP
- Overlaps
- TRAF3IP3
- Location
- 1:209760056
- Nucleotide Change
- C>T
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- (GRCh38)1:209760056C>T
- HGVS.c name
- ENSEMBL:ENST00000367024.5:c.17C>T
- ENSEMBL:ENST00000367025.8:c.17C>T
- HGVS.p name
- ENSP00000355991:p.Pro6Leu
- ENSP00000355992:p.Pro6Leu
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr1:209756032...209782320 (26.29 kb)
- Assembly version
- Not Available
- Viewer Help
Data currently unavailable; sequence viewer under construction