Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs185381772
- Species
- Homo sapiens
- Symbol
- rs185381772
- Category
- Variant
- Variant type
- SNP
- Overlaps
- KIAA0825
- Location
- 5:94396384
- Nucleotide Change
- A>T
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- (GRCh38)5:94396384A>T
- HGVS.c name
- ENSEMBL:ENST00000513200.7:c.3013T>A
- RefSeq:NM_001385713.1:c.3028T>A
- HGVS.p name
- ENSP00000424618:p.Phe1005Ile
- NP_001372642:p.Phe1010Ile
- 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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