Version: 8.1.0Date: Fri Apr 18 2025
Allele/Variant
rs768069468
- Species
- Homo sapiens
- Symbol
- rs768069468
- Category
- Variant
- Variant type
- SNP
- Overlaps
- FUCA1
- Location
- 1:23865498
- Nucleotide Change
- G>A
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- NC_000001.11:g.23865498G>A
- HGVS.c name
- ENSEMBL:ENST00000374479.4:c.517C>T
- RefSeq:NM_000147.5:c.517C>T
- HGVS.p name
- ENSP00000363603:p.Arg173Trp
- NP_000138:p.Arg173Trp
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr1:23845077...23868290 (23.21 kb)
- Assembly version
- Not Available
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