Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs200923377
- Species
- Homo sapiens
- Symbol
- rs200923377
- Category
- Variant
- Variant type
- SNP
- Overlaps
- CFAP97
- Location
- 4:185164065
- Nucleotide Change
- G>A
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- (GRCh38)4:185164065G>A
- HGVS.c name
- ENSEMBL:ENST00000458385.7:c.1435C>T
- RefSeq:XM_017008484.3:c.1435C>T
- HGVS.p name
- ENSP00000409964:p.Arg479Trp
- XP_016863973:p.Arg479Trp
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr4:185159665...185210248 (50.58 kb)
- Assembly version
- Not Available
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