Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs776400117
- Species
- Homo sapiens
- Symbol
- rs776400117
- Category
- Variant
- Variant type
- SNP
- Overlaps
- SLC16A13
- Location
- 17:7038467
- Nucleotide Change
- C>T
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- (GRCh38)17:7038467C>T
- HGVS.c name
- ENSEMBL:ENST00000308027.7:c.659C>T
- RefSeq:NM_201566.3:c.659C>T
- HGVS.p name
- ENSP00000309751:p.Thr220Ile
- NP_963860:p.Thr220Ile
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr17:7036015...7040117 (4.10 kb)
- Assembly version
- Not Available
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