Version: 8.1.0Date: Fri Apr 18 2025
Allele/Variant
rs751004054
- Species
- Homo sapiens
- Symbol
- rs751004054
- Category
- Variant
- Variant type
- SNP
- Overlaps
- TRAF3IP3
- Location
- 1:209777359
- Nucleotide Change
- A>G
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- (GRCh38)1:209777359A>G
- HGVS.c name
- ENSEMBL:ENST00000367023.5:c.269A>G
- ENSEMBL:ENST00000367024.5:c.1061A>G
- HGVS.p name
- ENSP00000355990:p.Asp90Gly
- ENSP00000355991:p.Asp354Gly
- 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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