Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs779593952
- Species
- Homo sapiens
- Symbol
- rs779593952
- Category
- Variant
- Variant type
- SNP
- Overlaps
- TARBP1
- Location
- 1:234406032
- Nucleotide Change
- C>G
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- (GRCh38)1:234406032C>G
- HGVS.c name
- ENSEMBL:ENST00000040877.2:c.3860G>C
- ENSEMBL:ENST00000462259.5:n.349G>C
- HGVS.p name
- ENSP00000040877:p.Arg1287Pro
- XP_016857685:p.Arg544Pro
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr1:234391313...234479179 (87.87 kb)
- Assembly version
- Not Available
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