Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs1442358772
- Species
- Homo sapiens
- Symbol
- rs1442358772
- Category
- Variant
- Variant type
- SNP
- Overlaps
- KIAA0825
- Location
- 5:94520895
- Nucleotide Change
- T>C
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- NC_000005.10:g.94520895T>C
- HGVS.c name
- ENSEMBL:ENST00000329378.7:c.323A>G
- ENSEMBL:ENST00000513200.7:c.323A>G
- HGVS.p name
- ENSP00000331385:p.Gln108Arg
- ENSP00000424618:p.Gln108Arg
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr5:94150851...94618604 (467.75 kb)
- Assembly version
- Not Available
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