Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs146590511
- Species
- Homo sapiens
- Symbol
- rs146590511
- Category
- Variant
- Variant type
- SNP
- Overlaps
- PACS2
- Location
- 14:105392750
- Nucleotide Change
- G>A
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- (GRCh38)14:105392750G>A
- HGVS.c name
- ENSEMBL:ENST00000325438.12:c.2342G>A
- ENSEMBL:ENST00000430725.6:c.2117G>A
- HGVS.p name
- ENSP00000321834:p.Arg781Gln
- ENSP00000393524:p.Arg706Gln
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr14:105300563...105398147 (97.58 kb)
- Assembly version
- Not Available
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