Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs770433938
- Species
- Homo sapiens
- Symbol
- rs770433938
- Category
- Variant
- Variant type
- SNP
- Overlaps
- GAL3ST4
- Location
- 7:100160700
- Nucleotide Change
- T>A
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- (GRCh38)7:100160700T>A
- HGVS.c name
- ENSEMBL:ENST00000360039.9:c.689A>T
- ENSEMBL:ENST00000411994.1:c.385A>T
- HGVS.p name
- ENSP00000353142:p.His230Leu
- ENSP00000399066:p.Ile129Phe
- 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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