Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs1031910707
- Species
- Homo sapiens
- Symbol
- rs1031910707
- Category
- Variant
- Variant type
- SNP
- Overlaps
- TRAF3IP3
- Location
- 1:209777484
- Nucleotide Change
- C>A
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- NC_000001.11:g.209777484C>A
- HGVS.c name
- ENSEMBL:ENST00000367023.5:c.394C>A
- ENSEMBL:ENST00000367024.5:c.1186C>A
- HGVS.p name
- ENSP00000355990:p.Gln132Lys
- ENSP00000355991:p.Gln396Lys
- 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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