Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs748859836
- Species
- Homo sapiens
- Symbol
- rs748859836
- Category
- Variant
- Variant type
- SNP
- Overlaps
- CLK4
- Location
- 5:178613479
- Nucleotide Change
- T>C
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- (GRCh38)5:178613479T>C
- HGVS.c name
- ENSEMBL:ENST00000316308.9:c.820A>G
- ENSEMBL:ENST00000519132.5:n.785A>G
- HGVS.p name
- ENSP00000316948:p.Ile274Val
- ENSP00000479788:p.Ile274Val
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr5:178602664...178630615 (27.95 kb)
- Assembly version
- Not Available
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