Version: 8.1.0Date: Fri Apr 18 2025
Allele/Variant
rs238982632
- Species
- Mus musculus
- Symbol
- rs238982632
- Category
- Variant
- Variant type
- SNP
- Overlaps
- Clu
- Location
- 14:66213478
- Nucleotide Change
- T>G
- Most Severe Consequence
- See all consequences
- intron variant
- HGVS.g name
- NC_000080.7:g.66213478T>G
- HGVS.c name
- ENSEMBL:ENSMUST00000022616.1:c.826+37T>G
- RefSeq:NM_001422221.1:c.826+37T>G
- HGVS.p name
- Not Available
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr14:66206093...66218992 (12.90 kb)
- Assembly version
- Not Available
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