Version: 8.1.0Date: Fri Apr 18 2025
Allele/Variant
rs375478163
- Species
- Homo sapiens
- Symbol
- rs375478163
- Category
- Variant
- Variant type
- SNP
- Overlaps
- NEIL3
- Location
- 4:177310010
- Nucleotide Change
- C>T
- Most Severe Consequence
- See all consequences
- synonymous variant
- HGVS.g name
- (GRCh38)4:177310010C>T
- HGVS.c name
- ENSEMBL:ENST00000264596.4:c.57C>T
- ENSEMBL:ENST00000513321.1:n.108C>T
- HGVS.p name
- ENSP00000264596:p.Leu19=
- NP_060718:p.Leu19=
- 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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