Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs1167723751
- Species
- Homo sapiens
- Symbol
- rs1167723751
- Category
- Variant
- Variant type
- SNP
- Overlaps
- ODAD2
- Location
- 10:27860633
- Nucleotide Change
- C>T
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- NC_000010.11:g.27860633C>T
- HGVS.c name
- ENSEMBL:ENST00000305242.10:c.3013G>A
- ENSEMBL:ENST00000671855.1:c.32G>A
- HGVS.p name
- ENSP00000306410:p.Ala1005Thr
- ENSP00000499983:p.Ala697Thr
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr10:27775186...27999675 (224.49 kb)
- Assembly version
- Not Available
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