Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs74441001
- Species
- Homo sapiens
- Symbol
- rs74441001
- Category
- Variant
- Variant type
- SNP
- Overlaps
- COX20
- Location
- 1:244835450
- Nucleotide Change
- C>T
- Most Severe Consequence
- See all consequences
- intron variant
- HGVS.g name
- (GRCh38)1:244835450C>T
- HGVS.c name
- RefSeq:NM_001312871.1:c.-239-26C>T
- HGVS.p name
- Not Available
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr1:244835306...244845063 (9.76 kb)
- Assembly version
- Not Available
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