Version: 8.1.0Date: Fri Apr 18 2025
Allele/Variant
rs1175330866
- Species
- Homo sapiens
- Symbol
- rs1175330866
- Category
- Variant
- Variant type
- SNP
- Overlaps
- KMT2C
- Location
- 7:152176862
- Nucleotide Change
- T>A
- Most Severe Consequence
- See all consequences
- stop lost
- HGVS.g name
- NC_000007.14:g.152176862T>A
- HGVS.c name
- ENSEMBL:ENST00000262189.11:c.8591A>T
- ENSEMBL:ENST00000355193.1:c.8810A>T
- HGVS.p name
- ENSP00000262189:p.Asp2864Val
- ENSP00000347325:p.Asp2937Val
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr7:152134922...152436644 (301.72 kb)
- Assembly version
- Not Available
- Viewer Help
Data currently unavailable; sequence viewer under construction