Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs2100658801
- Species
- Homo sapiens
- Symbol
- rs2100658801
- Category
- Variant
- Variant type
- SNP
- Overlaps
- MYSM1
- Location
- 1:58685231
- Nucleotide Change
- C>T
- Most Severe Consequence
- See all consequences
- stop gained
- HGVS.g name
- (GRCh38)1:58685231C>T
- HGVS.c name
- ENSEMBL:ENST00000401044.7:n.179G>A
- ENSEMBL:ENST00000472487.6:c.420G>A
- HGVS.p name
- ENSP00000418734:p.Trp140Ter
- ENSP00000499373:p.Trp140Ter
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr1:58643440...58700090 (56.65 kb)
- Assembly version
- Not Available
- Viewer Help
Data currently unavailable; sequence viewer under construction