Version: 8.1.0
Date: Fri Apr 18 2025
rs48975859
Variant overlaps Med8
Mus musculus
SummaryVariant Molecular Consequences
Allele/Variant

rs48975859

Species
Mus musculus
Symbol
rs48975859
Category
Variant
Variant type
SNP
Overlaps
Med8
Location
4:118267885
Nucleotide Change
A>C
Most Severe Consequence
  • intron variant
See all consequences
HGVS.g name
  • NC_000070.7:g.118267885A>C
HGVS.c name
  • ENSEMBL:ENSMUST00000019229.1:c.7-197A>C
  • ENSEMBL:ENSMUST00000073881.1:c.-309-197A>C
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:ENSMUST00000019229
protein_codingIntron 1/6
  • intron variant
ENSEMBL:ENSMUST00000073881
protein_codingIntron 1/7
  • intron variant
ENSEMBL:ENSMUST00000084319
protein_codingIntron 1/6
  • intron variant
ENSEMBL:ENSMUST00000106384
protein_codingIntron 1/7
  • intron variant
ENSEMBL:ENSMUST00000126089
protein_codingIntron 1/3
  • intron variant
ENSEMBL:ENSMUST00000130421
transcriptIntron 1/5
  • intron variant
ENSEMBL:ENSMUST00000144577
protein_codingIntron 1/4
  • intron variant
ENSEMBL:ENSMUST00000152633
transcriptExon 1/2
  • non coding transcript exon variant
RefSeq:NM_001290688.1
protein_codingIntron 1/6
  • intron variant
RefSeq:NM_020000.3
protein_codingIntron 1/6
  • intron variant
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