Allele/Variant

rs197903638

Species
Rattus norvegicus
Symbol
rs197903638
Category
Variant
Variant type
SNP
Overlaps
Greb1l
Location
18:1414861
Nucleotide Change
G>A
Most Severe Consequence
  • intron variant
See all consequences
HGVS.g name
  • (mRatBN7.2)18:1414861G>A
HGVS.c name
  • ENSEMBL:ENSRNOT00000033468.7:c.-111+22018G>A
  • RefSeq:XM_039097270.2:c.-111+22018G>A
HGVS.p name
Not Available
Synonyms
Not Available
Notes
Not Available
Cross references
Not Available
References
Not Available

Genome location
Assembly version
Not Available
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Variant Molecular Consequences