Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs1674869385
- Species
- Homo sapiens
- Symbol
- rs1674869385
- Category
- Variant
- Variant type
- SNP
- Overlaps
- ATRAID
- Location
- 2:27216904
- Nucleotide Change
- A>T
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- (GRCh38)2:27216904A>T
- HGVS.c name
- ENSEMBL:ENST00000380171.9:c.646A>T
- ENSEMBL:ENST00000405489.7:c.472A>T
- HGVS.p name
- ENSP00000369518:p.Ile216Phe
- ENSP00000384033:p.Ile158Phe
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr2:27212041...27217183 (5.14 kb)
- Assembly version
- Not Available
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