Version: 8.1.0Date: Fri Apr 18 2025
Allele/Variant
rs775412122
- Species
- Homo sapiens
- Symbol
- rs775412122
- Category
- Variant
- Variant type
- SNP
- Overlaps
- DGCR6L
- Location
- 22:20314785
- Nucleotide Change
- T>G
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- NC_000022.11:g.20314785T>G
- HGVS.c name
- ENSEMBL:ENST00000248879.8:c.553A>C
- ENSEMBL:ENST00000405465.3:c.439A>C
- HGVS.p name
- ENSP00000248879:p.Lys185Gln
- ENSP00000386052:p.Lys147Gln
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr22:20314238...20320080 (5.84 kb)
- Assembly version
- Not Available
- Viewer Help
Data currently unavailable; sequence viewer under construction