Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs51789350
- Species
- Mus musculus
- Symbol
- rs51789350
- Category
- Variant
- Variant type
- SNP
- Overlaps
- Pdhb
- Location
- 14:14299714
- Nucleotide Change
- C>T
- Most Severe Consequence
- See all consequences
- intron variant
- HGVS.g name
- (GRCm39)14:14299714C>T
- HGVS.c name
- ENSEMBL:ENSMUST00000022268.1:c.589+102C>T
- ENSEMBL:ENSMUST00000224466.1:n.353-240C>T
- HGVS.p name
- Not Available
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr14:14296748...14303777 (7.03 kb)
- Assembly version
- Not Available
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