Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs772347149
- Species
- Homo sapiens
- Symbol
- rs772347149
- Category
- Variant
- Variant type
- SNP
- Overlaps
- PRKCE
- Location
- 2:46007602
- Nucleotide Change
- C>T
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- NC_000002.12:g.46007602C>T
- HGVS.c name
- ENSEMBL:ENST00000306156.8:c.1204C>T
- ENSEMBL:ENST00000394874.1:c.373C>T
- HGVS.p name
- ENSP00000306124:p.Arg402Cys
- ENSP00000378341:p.Arg125Cys
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr2:45651279...46187990 (536.71 kb)
- Assembly version
- Not Available
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