Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs1474775371
- Species
- Homo sapiens
- Symbol
- rs1474775371
- Category
- Variant
- Variant type
- SNP
- Overlaps
- PRTFDC1
- Location
- 10:24942339
- Nucleotide Change
- A>T
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- (GRCh38)10:24942339A>T
- HGVS.c name
- ENSEMBL:ENST00000320152.11:c.146T>A
- ENSEMBL:ENST00000376376.3:c.146T>A
- HGVS.p name
- ENSP00000318602:p.Ile49Asn
- ENSP00000365556:p.Ile49Asn
- 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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