Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs1010090465
- Species
- Homo sapiens
- Symbol
- rs1010090465
- Category
- Variant
- Variant type
- SNP
- Overlaps
- TAS1R3
- Location
- 1:1332775
- Nucleotide Change
- G>A
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- (GRCh38)1:1332775G>A
- HGVS.c name
- ENSEMBL:ENST00000339381.6:c.1244G>A
- HGVS.p name
- ENSP00000344411:p.Cys415Tyr
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr1:1331280...1335314 (4.03 kb)
- Assembly version
- Not Available
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