Version: 8.0.0
Date: Tue Jan 28 2025
rs261211927
Variant overlaps Rtkn
Mus musculus
SummaryVariant Molecular Consequences
Allele/Variant

rs261211927

Species
Mus musculus
Symbol
rs261211927
Category
Variant
Variant type
SNP
Overlaps
Rtkn
Location
6:83126434
Nucleotide Change
T>C
Most Severe Consequence
  • intron variant
See all consequences
HGVS.g name
  • (GRCm39)6:83126434T>C
HGVS.c name
  • ENSEMBL:ENSMUST00000065512.1:c.756-11T>C
  • ENSEMBL:ENSMUST00000087938.1:c.717-11T>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:ENSMUST00000065512
protein_codingRtknIntron 6/11
  • intron variant
ENSEMBL:ENSMUST00000087938
protein_codingRtknIntron 6/11
  • intron variant
ENSEMBL:ENSMUST00000121093
protein_codingRtknIntron 7/12
  • intron variant
ENSEMBL:ENSMUST00000135490
protein_codingRtknIntron 6/6
  • intron variant
ENSEMBL:ENSMUST00000153148
protein_codingWdr54Exon 10/10
  • 3 prime UTR variant
RefSeq:NM_001136227.2
protein_codingRtknIntron 6/11
  • intron variant
RefSeq:NM_001355524.2
protein_codingRtknIntron 6/11
  • intron variant
RefSeq:NM_001355525.2
protein_codingRtknIntron 6/11
  • intron variant
RefSeq:NM_001410312.1
protein_codingRtknIntron 6/11
  • intron variant
RefSeq:NM_001410313.1
protein_codingRtknIntron 6/11
  • intron variant
Showing 1 - 10 of 23 rows
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