Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs749799203
- Species
- Homo sapiens
- Symbol
- rs749799203
- Category
- Variant
- Variant type
- SNP
- Overlaps
- TTC5
- Location
- 14:20296394
- Nucleotide Change
- G>A
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- (GRCh38)14:20296394G>A
- HGVS.c name
- ENSEMBL:ENST00000258821.8:c.692C>T
- ENSEMBL:ENST00000383029.7:n.628C>T
- HGVS.p name
- ENSP00000258821:p.Ala231Val
- NP_612385:p.Ala231Val
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr14:20256558...20305960 (49.40 kb)
- Assembly version
- Not Available
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