Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs199127216
- Species
- Rattus norvegicus
- Symbol
- rs199127216
- Category
- Variant
- Variant type
- SNP
- Overlaps
- Gltp
- Location
- 12:41911484
- Nucleotide Change
- C>T
- Most Severe Consequence
- See all consequences
- intron variant
- HGVS.g name
- (mRatBN7.2)12:41911484C>T
- HGVS.c name
- ENSEMBL:ENSRNOT00000001581.7:c.103+4150C>T
- RefSeq:NM_001134413.1:c.103+4150C>T
- HGVS.p name
- Not Available
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr12:41907144...41927321 (20.18 kb)
- Assembly version
- Not Available
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