Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs777894947
- Species
- Homo sapiens
- Symbol
- rs777894947
- Category
- Variant
- Variant type
- SNP
- Overlaps
- GAL3ST4
- Location
- 7:100166510
- Nucleotide Change
- G>T
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- NC_000007.14:g.100166510G>T
- HGVS.c name
- ENSEMBL:ENST00000360039.9:c.421C>A
- ENSEMBL:ENST00000411994.1:c.125+461C>A
- HGVS.p name
- ENSP00000353142:p.Leu141Met
- ENSP00000400451:p.Leu141Met
- 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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