Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs2134099850
- Species
- Homo sapiens
- Symbol
- rs2134099850
- Category
- Variant
- Variant type
- SNP
- Overlaps
- ODAD2
- Location
- 10:27936707
- Nucleotide Change
- A>T
- Most Severe Consequence
- See all consequences
- intron variant
- HGVS.g name
- NC_000010.11:g.27936707A>T
- HGVS.c name
- ENSEMBL:ENST00000305242.10:c.2252+19T>A
- ENSEMBL:ENST00000672841.1:c.1328+19T>A
- HGVS.p name
- Not Available
- 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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