Version: 8.1.0Date: Fri Apr 18 2025
Allele/Variant
rs149882271
- Species
- Homo sapiens
- Symbol
- rs149882271
- Category
- Variant
- Variant type
- SNP
- Overlaps
- COBLL1
- Location
- 2:164704960
- Nucleotide Change
- C>T
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- (GRCh38)2:164704960C>T
- HGVS.c name
- ENSEMBL:ENST00000342193.8:c.1142G>A
- ENSEMBL:ENST00000375458.6:c.1142G>A
- HGVS.p name
- ENSP00000341360:p.Arg381His
- ENSP00000364607:p.Arg381His
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr2:164653624...164843679 (190.06 kb)
- Assembly version
- Not Available
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