Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs754808999
- Species
- Homo sapiens
- Symbol
- rs754808999
- Category
- Variant
- Variant type
- SNP
- Overlaps
- ECPAS
- Location
- 9:111397057
- Nucleotide Change
- T>C
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- (GRCh38)9:111397057T>C
- HGVS.c name
- ENSEMBL:ENST00000259335.8:c.3283A>G
- ENSEMBL:ENST00000338205.9:c.2749A>G
- HGVS.p name
- ENSP00000259335:p.Thr1095Ala
- ENSP00000339889:p.Thr917Ala
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr9:111360685...111484745 (124.06 kb)
- Assembly version
- Not Available
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