Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs759881725
- Species
- Homo sapiens
- Symbol
- rs759881725
- Category
- Variant
- Variant type
- SNP
- Overlaps
- HAL
- Location
- 12:95976464
- Nucleotide Change
- T>C
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- (GRCh38)12:95976464T>C
- HGVS.c name
- ENSEMBL:ENST00000261208.8:c.1798A>G
- ENSEMBL:ENST00000538703.5:c.1763+134A>G
- HGVS.p name
- ENSP00000261208:p.Ile600Val
- ENSP00000446364:p.Ile392Val
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr12:95972662...95996365 (23.70 kb)
- Assembly version
- Not Available
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