Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs1134859517
- Species
- Mus musculus
- Symbol
- rs1134859517
- Category
- Variant
- Variant type
- SNP
- Overlaps
- Emx1
- Location
- 6:85165847
- Nucleotide Change
- C>T
- Most Severe Consequence
- See all consequences
- intron variant
- HGVS.g name
- (GRCm39)6:85165847C>T
- HGVS.c name
- ENSEMBL:ENSMUST00000045942.1:c.421+502C>T
- RefSeq:NM_010131.2:c.421+502C>T
- HGVS.p name
- Not Available
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr6:85164913...85181445 (16.53 kb)
- Assembly version
- Not Available
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