Version: 8.1.0Date: Fri Apr 18 2025
Allele/Variant
rs1734448457
- Species
- Homo sapiens
- Symbol
- rs1734448457
- Category
- Variant
- Variant type
- SNP
- Overlaps
- NEIL3
- Location
- 4:177310098
- Nucleotide Change
- G>T
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- NC_000004.12:g.177310098G>T
- HGVS.c name
- ENSEMBL:ENST00000264596.4:c.145G>T
- ENSEMBL:ENST00000513321.1:n.196G>T
- HGVS.p name
- ENSP00000264596:p.Val49Phe
- NP_060718:p.Val49Phe
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr4:177309874...177371268 (61.39 kb)
- Assembly version
- Not Available
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