Version: 8.1.0Date: Fri Apr 18 2025
Allele/Variant
rs146811375
- Species
- Homo sapiens
- Symbol
- rs146811375
- Category
- Variant
- Variant type
- SNP
- Overlaps
- ACBD7
- Location
- 10:15078998
- Nucleotide Change
- C>T
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- (GRCh38)10:15078998C>T
- HGVS.c name
- ENSEMBL:ENST00000356189.6:c.55G>A
- ENSEMBL:ENST00000496890.1:n.219G>A
- HGVS.p name
- ENSP00000367453:p.Ala19Thr
- NP_001034933:p.Ala19Thr
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr10:15075475...15088776 (13.30 kb)
- Assembly version
- Not Available
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