Version: 8.1.0Date: Fri Apr 18 2025
Allele/Variant
rs146174646
- Species
- Homo sapiens
- Symbol
- rs146174646
- Category
- Variant
- Variant type
- SNP
- Overlaps
- PRTFDC1
- Location
- 10:24849854
- Nucleotide Change
- T>C
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- NC_000010.11:g.24849854T>C
- HGVS.c name
- ENSEMBL:ENST00000320152.11:c.668A>G
- ENSEMBL:ENST00000376378.5:c.*18A>G
- HGVS.p name
- ENSP00000318602:p.Tyr223Cys
- NP_064585:p.Tyr223Cys
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr10:24848614...24952606 (103.99 kb)
- Assembly version
- Not Available
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