Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs3320939453
- Species
- Rattus norvegicus
- Symbol
- rs3320939453
- Category
- Variant
- Variant type
- SNP
- Overlaps
- Btbd7
- Location
- 6:121925115
- Nucleotide Change
- A>C
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- NC_051341.1:g.121925115A>C
- HGVS.c name
- ENSEMBL:ENSRNOT00000064914.4:c.2440T>G
- ENSEMBL:ENSRNOT00000081127.2:c.2890T>G
- HGVS.p name
- ENSRNOP00000062323:p.Ser814Ala
- ENSRNOP00000074965:p.Ser964Ala
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr6:121920365...122010114 (89.75 kb)
- Assembly version
- Not Available
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