Version: 8.1.0Date: Fri Apr 18 2025
Allele/Variant
rs1330861874
- Species
- Homo sapiens
- Symbol
- rs1330861874
- Category
- Variant
- Variant type
- SNP
- Overlaps
- COP1
- Location
- 1:176162970
- Nucleotide Change
- T>C
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- (GRCh38)1:176162970T>C
- HGVS.c name
- ENSEMBL:ENST00000308769.12:c.649A>G
- ENSEMBL:ENST00000367666.5:c.226A>G
- HGVS.p name
- ENSP00000310943:p.Ile217Val
- ENSP00000356638:p.Ile76Val
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr1:175944831...176207286 (262.46 kb)
- Assembly version
- Not Available
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