Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs50419566
- Species
- Mus musculus
- Symbol
- rs50419566
- Category
- Variant
- Variant type
- SNP
- Overlaps
- Snrpn
- Location
- 7:59654342
- Nucleotide Change
- T>C
- Most Severe Consequence
- See all consequences
- intron variant
- HGVS.g name
- (GRCm39)7:59654342T>C
- HGVS.c name
- ENSEMBL:ENSMUST00000059305.1:c.-389+442A>G
- ENSEMBL:ENSMUST00000098402.1:c.-388-5181A>G
- HGVS.p name
- Not Available
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr7:59632243...59789967 (157.72 kb)
- Assembly version
- Not Available
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