Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs1700769766
- Species
- Homo sapiens
- Symbol
- rs1700769766
- Category
- Variant
- Variant type
- SNP
- Overlaps
- SLC6A6
- Location
- 3:14472304
- Nucleotide Change
- G>T
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- (GRCh38)3:14472304G>T
- HGVS.c name
- ENSEMBL:ENST00000452151.1:c.63G>T
- ENSEMBL:ENST00000610642.4:n.1396G>T
- HGVS.p name
- ENSP00000399522:p.Trp21Cys
- ENSP00000480890:p.Gly399Val
- 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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