Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs779464556
- Species
- Homo sapiens
- Symbol
- rs779464556
- Category
- Variant
- Variant type
- SNP
- Overlaps
- CCL14
- Location
- 17:35986637
- Nucleotide Change
- C>T
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- (GRCh38)17:35986637C>T
- HGVS.c name
- ENSEMBL:ENST00000614009.1:c.-2040G>A
- ENSEMBL:ENST00000618404.5:c.13G>A
- HGVS.p name
- ENSP00000479097:p.Val5Met
- ENSP00000481023:p.Val5Met
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr17:35983288...35987004 (3.72 kb)
- Assembly version
- Not Available
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