Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs777459977
- Species
- Homo sapiens
- Symbol
- rs777459977
- Category
- Variant
- Variant type
- SNP
- Overlaps
- KIAA0825
- Location
- 5:94440063
- Nucleotide Change
- G>T
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- NC_000005.10:g.94440063G>T
- HGVS.c name
- ENSEMBL:ENST00000504117.1:n.1263C>A
- ENSEMBL:ENST00000513200.7:c.2416C>A
- HGVS.p name
- ENSP00000424618:p.Pro806Thr
- NP_001372642:p.Pro806Thr
- 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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