Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs780712348
- Species
- Homo sapiens
- Symbol
- rs780712348
- Category
- Variant
- Variant type
- SNP
- Overlaps
- NOXRED1
- Location
- 14:77422828
- Nucleotide Change
- C>T
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- (GRCh38)14:77422828C>T
- HGVS.c name
- ENSEMBL:ENST00000380835.7:c.62G>A
- ENSEMBL:ENST00000555603.1:c.62G>A
- HGVS.p name
- ENSP00000370215:p.Arg21His
- ENSP00000450597:p.Arg21His
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr14:77394021...77426013 (31.99 kb)
- Assembly version
- Not Available
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