Version: 8.1.0Date: Fri Apr 18 2025
Allele/Variant
rs13462799
- Species
- Mus musculus
- Symbol
- rs13462799
- Category
- Variant
- Variant type
- SNP
- Overlaps
- Spint1
- Location
- 2:119068675
- Nucleotide Change
- T>C
- Most Severe Consequence
- See all consequences
- synonymous variant
- HGVS.g name
- (GRCm39)2:119068675T>C
- HGVS.c name
- ENSEMBL:ENSMUST00000028783.1:c.408T>C
- ENSEMBL:ENSMUST00000110816.1:c.408T>C
- HGVS.p name
- ENSEMBL:ENSMUSP00000028783:p.Thr136=
- ENSEMBL:ENSMUSP00000106440:p.Thr136=
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr2:119067841...119079995 (12.15 kb)
- Assembly version
- Not Available
- Viewer Help
Data currently unavailable; sequence viewer under construction