Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs10889548
- Species
- Homo sapiens
- Symbol
- rs10889548
- Category
- Variant
- Variant type
- SNP
- Overlaps
- DNAJC6
- Location
- 1:65398537
- Nucleotide Change
- G>T
- Most Severe Consequence
- See all consequences
- intron variant
- HGVS.g name
- (GRCh38)1:65398537G>T
- HGVS.c name
- ENSEMBL:ENST00000263441.11:c.1829-276G>T
- ENSEMBL:ENST00000371069.5:c.2039-276G>T
- HGVS.p name
- Not Available
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr1:65248219...65415871 (167.65 kb)
- Assembly version
- Not Available
- Viewer Help
Data currently unavailable; sequence viewer under construction