Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs138676697
- Species
- Homo sapiens
- Symbol
- rs138676697
- Category
- Variant
- Variant type
- SNP
- Overlaps
- TRAF3IP3
- Location
- 1:209760304
- Nucleotide Change
- C>A
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- (GRCh38)1:209760304C>A
- HGVS.c name
- ENSEMBL:ENST00000367024.5:c.265C>A
- ENSEMBL:ENST00000367025.8:c.265C>A
- HGVS.p name
- ENSP00000355991:p.Pro89Thr
- ENSP00000355992:p.Pro89Thr
- 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
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