Allele/Variant
rs3320066202
- Species
- Rattus norvegicus
- Symbol
- rs3320066202
- Category
- Variant
- Variant type
- SNP
- Overlaps
- Kmt2c
- Location
- 4:9721753
- Nucleotide Change
- T>A
- Most Severe Consequence
- See all consequences
- intron variant
- HGVS.g name
- NC_051339.1:g.9721753T>A
- HGVS.c name
- ENSEMBL:ENSRNOT00000093625.2:c.1009+1582T>A
- ENSEMBL:ENSRNOT00000101551.1:c.1012+1582T>A
- HGVS.p name
- Not Available
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr4:9609627...9834787 (225.16 kb)
- Assembly version
- Not Available
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