Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs49661906
- Species
- Mus musculus
- Symbol
- rs49661906
- Category
- Variant
- Variant type
- SNP
- Overlaps
- Gtf2h2
- Location
- 13:100597849
- Nucleotide Change
- G>T
- Most Severe Consequence
- See all consequences
- intron variant
- HGVS.g name
- NC_000079.7:g.100597849G>T
- HGVS.c name
- ENSEMBL:ENSMUST00000145266.1:c.*101+507C>A
- ENSEMBL:ENSMUST00000231227.1:n.209+507C>A
- HGVS.p name
- Not Available
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr13:100596726...100629087 (32.36 kb)
- Assembly version
- Not Available
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