Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs201998409
- Species
- Homo sapiens
- Symbol
- rs201998409
- Category
- Variant
- Variant type
- SNP
- Overlaps
- RO60
- Location
- 1:193076994
- Nucleotide Change
- C>T
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- (GRCh38)1:193076994C>T
- HGVS.c name
- ENSEMBL:ENST00000367441.1:c.1030C>T
- ENSEMBL:ENST00000367446.7:c.1030C>T
- HGVS.p name
- ENSP00000356411:p.Arg344Cys
- ENSP00000356416:p.Arg344Cys
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr1:193059454...193091777 (32.32 kb)
- Assembly version
- Not Available
- Viewer Help
Data currently unavailable; sequence viewer under construction