Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs370288680
- Species
- Homo sapiens
- Symbol
- rs370288680
- Category
- Variant
- Variant type
- SNP
- Overlaps
- PRPF6
- Location
- 20:63983032
- Nucleotide Change
- G>C
- Most Severe Consequence
- See all consequences
- intron variant
- HGVS.g name
- (GRCh38)20:63983032G>C
- HGVS.c name
- ENSEMBL:ENST00000266079.5:c.72-15G>C
- RefSeq:XR_007067448.1:n.186-15G>C
- HGVS.p name
- Not Available
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr20:63981132...64033100 (51.97 kb)
- Assembly version
- Not Available
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