Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs986607232
- Species
- Homo sapiens
- Symbol
- rs986607232
- Category
- Variant
- Variant type
- SNP
- Overlaps
- ZDHHC13
- Location
- 11:19150748
- Nucleotide Change
- A>G
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- (GRCh38)11:19150748A>G
- HGVS.c name
- ENSEMBL:ENST00000399351.7:c.151A>G
- ENSEMBL:ENST00000446113.7:c.541A>G
- HGVS.p name
- ENSP00000382288:p.Asn51Asp
- ENSP00000400113:p.Asn181Asp
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr11:19117099...19176422 (59.32 kb)
- Assembly version
- Not Available
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