Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs217509231
- Species
- Mus musculus
- Symbol
- rs217509231
- Category
- Variant
- Variant type
- SNP
- Overlaps
- Prrt2
- Location
- 7:126619952
- Nucleotide Change
- T>C
- Most Severe Consequence
- See all consequences
- intron variant
- HGVS.g name
- (GRCm39)7:126619952T>C
- HGVS.c name
- ENSEMBL:ENSMUST00000159916.1:c.-65+225A>G
- ENSEMBL:ENSMUST00000161728.1:n.85+225A>G
- HGVS.p name
- Not Available
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr7:126616703...126620383 (3.68 kb)
- Assembly version
- Not Available
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