Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs139577335
- Species
- Homo sapiens
- Symbol
- rs139577335
- Category
- Variant
- Variant type
- SNP
- Overlaps
- USPL1
- Location
- 13:30659177
- Nucleotide Change
- C>T
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- (GRCh38)13:30659177C>T
- HGVS.c name
- ENSEMBL:ENST00000255304.9:c.3100C>T
- ENSEMBL:ENST00000614860.1:c.2113C>T
- HGVS.p name
- ENSP00000255304:p.Pro1034Ser
- ENSP00000480656:p.Pro705Ser
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr13:30617693...30660770 (43.08 kb)
- Assembly version
- Not Available
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