Version: 8.1.0Date: Fri Apr 18 2025
Allele/Variant
rs107984705
- Species
- Mus musculus
- Symbol
- rs107984705
- Category
- Variant
- Variant type
- SNP
- Overlaps
- Ccdc8
- Location
- 7:16729510
- Nucleotide Change
- A>T
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- (GRCm39)7:16729510A>T
- HGVS.c name
- ENSEMBL:ENSMUST00000094805.1:c.998A>T
- ENSEMBL:ENSMUST00000247846.1:c.1208A>T
- HGVS.p name
- ENSEMBL:ENSMUSP00000092399:p.Asp333Val
- ENSEMBL:ENSMUSP00000159532:p.Asp403Val
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr7:16727827...16731440 (3.61 kb)
- Assembly version
- Not Available
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