Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs262985994
- Species
- Mus musculus
- Symbol
- rs262985994
- Category
- Variant
- Variant type
- SNP
- Overlaps
- Ncf2
- Location
- 1:152684148
- Nucleotide Change
- T>C
- Most Severe Consequence
- See all consequences
- intron variant
- HGVS.g name
- (GRCm39)1:152684148T>C
- HGVS.c name
- ENSEMBL:ENSMUST00000027754.1:c.174+192T>C
- ENSEMBL:ENSMUST00000186568.1:c.174+192T>C
- HGVS.p name
- Not Available
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr1:152675945...152712742 (36.80 kb)
- Assembly version
- Not Available
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