Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs13491020
- Species
- Mus musculus
- Symbol
- rs13491020
- Category
- Variant
- Variant type
- SNP
- Overlaps
- Traf3ip3
- Location
- 1:192876681
- Nucleotide Change
- A>T
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- (GRCm39)1:192876681A>T
- HGVS.c name
- ENSEMBL:ENSMUST00000043550.1:c.621T>A
- ENSEMBL:ENSMUST00000192020.1:c.621T>A
- HGVS.p name
- ENSEMBL:ENSMUSP00000040977:p.His207Gln
- ENSEMBL:ENSMUSP00000141698:p.His207Gln
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr1:192857812...192883854 (26.04 kb)
- Assembly version
- Not Available
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