Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs774906046
- Species
- Homo sapiens
- Symbol
- rs774906046
- Category
- Variant
- Variant type
- SNP
- Overlaps
- SLC6A6
- Location
- 3:14447780
- Nucleotide Change
- C>A
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- (GRCh38)3:14447780C>A
- HGVS.c name
- ENSEMBL:ENST00000610642.4:n.888C>A
- ENSEMBL:ENST00000613060.4:c.866C>A
- HGVS.p name
- ENSP00000480890:p.Ser188Tyr
- ENSP00000481625:p.Ser289Tyr
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr3:14402576...14489349 (86.77 kb)
- Assembly version
- Not Available
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