Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs29464158
- Species
- Mus musculus
- Symbol
- rs29464158
- Category
- Variant
- Variant type
- SNP
- Overlaps
- Chct1
- Location
- 11:85059276
- Nucleotide Change
- G>T
- Most Severe Consequence
- See all consequences
- intron variant
- HGVS.g name
- (GRCm39)11:85059276G>T
- HGVS.c name
- RefSeq:XM_011249281.4:c.7-4384G>T
- RefSeq:XM_030246376.2:c.-1-5567G>T
- HGVS.p name
- Not Available
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr11:85061230...85071971 (10.74 kb)
- Assembly version
- Not Available
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