Version: 8.1.0Date: Fri Apr 18 2025
Allele/Variant
rs141603902
- Species
- Homo sapiens
- Symbol
- rs141603902
- Category
- Variant
- Variant type
- SNP
- Overlaps
- DESI2
- Location
- 1:244705772
- Nucleotide Change
- C>T
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- (GRCh38)1:244705772C>T
- HGVS.c name
- ENSEMBL:ENST00000263831.11:c.469C>T
- ENSEMBL:ENST00000302550.16:c.568C>T
- HGVS.p name
- ENSP00000263831:p.Arg157Cys
- ENSP00000306528:p.Arg190Cys
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr1:244653103...244709033 (55.93 kb)
- Assembly version
- Not Available
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