Version: 8.1.0Date: Fri Apr 18 2025
Allele/Variant
rs149092760
- Species
- Homo sapiens
- Symbol
- rs149092760
- Category
- Variant
- Variant type
- SNP
- Overlaps
- GAL3ST4
- Location
- 7:100166493
- Nucleotide Change
- A>T
- Most Severe Consequence
- See all consequences
- intron variant
- HGVS.g name
- NC_000007.14:g.100166493A>T
- HGVS.c name
- ENSEMBL:ENST00000360039.9:c.429+9T>A
- ENSEMBL:ENST00000411994.1:c.125+478T>A
- HGVS.p name
- Not Available
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr7:100159244...100168617 (9.37 kb)
- Assembly version
- Not Available
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