Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs147409941
- Species
- Homo sapiens
- Symbol
- rs147409941
- Category
- Variant
- Variant type
- SNP
- Overlaps
- TTC5
- Location
- 14:20295725
- Nucleotide Change
- T>C
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- (GRCh38)14:20295725T>C
- HGVS.c name
- ENSEMBL:ENST00000258821.8:c.826A>G
- ENSEMBL:ENST00000383029.7:n.762A>G
- HGVS.p name
- ENSP00000258821:p.Ser276Gly
- NP_612385:p.Ser276Gly
- 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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