Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs3321183723
- Species
- Rattus norvegicus
- Symbol
- rs3321183723
- Category
- Variant
- Variant type
- SNP
- Overlaps
- C1ql4
- Location
- 7:130246268
- Nucleotide Change
- G>T
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- NC_051342.1:g.130246268G>T
- HGVS.c name
- ENSEMBL:ENSRNOT00000081784.2:c.322C>A
- RefSeq:NM_001271242.2:c.322C>A
- HGVS.p name
- ENSRNOP00000069930:p.Pro108Thr
- NP_001258171:p.Pro108Thr
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr7:130243606...130246678 (3.07 kb)
- Assembly version
- Not Available
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