Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs114062874
- Species
- Homo sapiens
- Symbol
- rs114062874
- Category
- Variant
- Variant type
- SNP
- Overlaps
- CDC20B
- Location
- 5:55161140
- Nucleotide Change
- C>T
- Most Severe Consequence
- See all consequences
- synonymous variant
- HGVS.g name
- NC_000005.10:g.55161140C>T
- HGVS.c name
- ENSEMBL:ENST00000296733.5:c.126+11448G>A
- ENSEMBL:ENST00000296734.6:c.204+744C>T
- HGVS.p name
- ENSP00000423822:p.Arg117=
- ENSP00000427466:p.Arg66=
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr5:55112971...55173177 (60.21 kb)
- Assembly version
- Not Available
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