Version: 8.0.0
Date: Tue Jan 28 2025
rs213787702
Variant overlaps Nop58
Mus musculus
SummaryVariant Molecular Consequences
Allele/Variant

rs213787702

Species
Mus musculus
Symbol
rs213787702
Category
Variant
Variant type
SNP
Overlaps
Nop58
Location
1:59735723
Nucleotide Change
A>G
Most Severe Consequence
  • intron variant
See all consequences
HGVS.g name
  • (GRCm39)1:59735723A>G
HGVS.c name
  • ENSEMBL:ENSMUST00000027174.1:c.297+465A>G
  • ENSEMBL:ENSMUST00000189327.1:c.*291+465A>G
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

Sequence feature
Sequence feature type
Associated gene
Location
Molecular consequence
Codon and amino acid change
ENSEMBL:ENSMUST00000027174
protein_codingNop58Intron 4/12
  • intron variant
ENSEMBL:ENSMUST00000189327
protein_codingNop58Intron 5/5
  • intron variant
ENSEMBL:ENSMUST00000189919
protein_codingNop58Intron 1/5
  • intron variant
ENSEMBL:ENSMUST00000191142
protein_codingNop58Intron 4/14
  • intron variant
RefSeq:NM_001420730.1
protein_codingNop58Intron 4/14
  • intron variant
RefSeq:NM_001420731.1
protein_codingNop58Intron 4/13
  • intron variant
RefSeq:NM_001420732.1
protein_codingNop58Intron 4/14
  • intron variant
RefSeq:NM_001420733.1
protein_codingNop58Intron 5/15
  • intron variant
RefSeq:NM_001420734.1
protein_codingNop58Intron 5/15
  • intron variant
RefSeq:NM_001420735.1
protein_codingNop58Intron 3/13
  • intron variant
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