Version: 8.1.0Date: Fri Apr 18 2025
Allele/Variant
rs49774298
- Species
- Mus musculus
- Symbol
- rs49774298
- Category
- Variant
- Variant type
- SNP
- Overlaps
- Nrn1
- Location
- 13:36916863
- Nucleotide Change
- T>C
- Most Severe Consequence
- See all consequences
- intron variant
- HGVS.g name
- (GRCm39)13:36916863T>C
- HGVS.c name
- ENSEMBL:ENSMUST00000037623.1:c.55+1347A>G
- ENSEMBL:ENSMUST00000224960.1:c.55+1347A>G
- HGVS.p name
- Not Available
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr13:36909596...36918451 (8.86 kb)
- Assembly version
- Not Available
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