Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs769969649
- Species
- Homo sapiens
- Symbol
- rs769969649
- Category
- Variant
- Variant type
- SNP
- Overlaps
- ZDHHC13
- Location
- 11:19147651
- Nucleotide Change
- A>T
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- (GRCh38)11:19147651A>T
- HGVS.c name
- ENSEMBL:ENST00000399351.7:c.-39A>T
- ENSEMBL:ENST00000446113.7:c.352A>T
- HGVS.p name
- ENSP00000400113:p.Thr118Ser
- XP_011518496:p.Thr138Ser
- 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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