Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs372583992
- Species
- Homo sapiens
- Symbol
- rs372583992
- Category
- Variant
- Variant type
- SNP
- Overlaps
- GATB
- Location
- 4:151701363
- Nucleotide Change
- T>G
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- (GRCh38)4:151701363T>G
- HGVS.c name
- ENSEMBL:ENST00000263985.11:c.1163A>C
- ENSEMBL:ENST00000503160.5:n.1038A>C
- HGVS.p name
- ENSP00000263985:p.Tyr388Ser
- ENSP00000426859:p.Tyr347Ser
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr4:151670504...151761007 (90.50 kb)
- Assembly version
- Not Available
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