Version: 8.1.0
Date: Fri Apr 18 2025
rs250786068
Variant overlaps Snx7
Mus musculus
SummaryVariant Molecular Consequences
Allele/Variant

rs250786068

Species
Mus musculus
Symbol
rs250786068
Category
Variant
Variant type
SNP
Overlaps
Snx7
Location
3:117659258
Nucleotide Change
G>C
Most Severe Consequence
  • intron variant
See all consequences
HGVS.g name
  • (GRCm39)3:117659258G>C
HGVS.c name
  • ENSEMBL:ENSMUST00000029639.1:c.162+3135C>G
  • ENSEMBL:ENSMUST00000167877.1:c.78+3135C>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:ENSMUST00000029639
protein_codingIntron 1/8
  • intron variant
ENSEMBL:ENSMUST00000167877
protein_codingIntron 1/7
  • intron variant
ENSEMBL:ENSMUST00000169812
protein_codingIntron 1/7
  • intron variant
RefSeq:NM_001190156.1
protein_codingIntron 1/7
  • intron variant
RefSeq:NM_029655.3
protein_codingIntron 1/8
  • intron variant
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