Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs780263411
- Species
- Homo sapiens
- Symbol
- rs780263411
- Category
- Variant
- Variant type
- SNP
- Overlaps
- SYNE1
- Location
- 6:152122672
- Nucleotide Change
- T>A
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- NC_000006.12:g.152122672T>A
- HGVS.c name
- ENSEMBL:ENST00000341594.9:c.24943A>T
- ENSEMBL:ENST00000347037.9:n.2906A>T
- HGVS.p name
- :p.His902Leu
- ENSP00000341887:p.Thr8315Ser
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr6:152121687...152637801 (516.11 kb)
- Assembly version
- Not Available
- Viewer Help
Data currently unavailable; sequence viewer under construction