Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs1280841182
- Species
- Homo sapiens
- Symbol
- rs1280841182
- Category
- Variant
- Variant type
- SNP
- Overlaps
- ABCD4
- Location
- 14:74295878
- Nucleotide Change
- T>C
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- NC_000014.9:g.74295878T>C
- HGVS.c name
- ENSEMBL:ENST00000356924.9:c.644A>G
- ENSEMBL:ENST00000460308.6:n.659A>G
- HGVS.p name
- ENSP00000349396:p.Gln215Arg
- ENSP00000451770:p.Arg175Gly
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr14:74285269...74303055 (17.79 kb)
- Assembly version
- Not Available
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