Version: 8.0.0
Date: Tue Jan 28 2025
rs49990387
Variant overlaps Fgf11
Mus musculus
SummaryVariant Molecular Consequences
Allele/Variant

rs49990387

Species
Mus musculus
Symbol
rs49990387
Category
Variant
Variant type
SNP
Overlaps
Fgf11
Location
11:69689200
Nucleotide Change
C>T
Most Severe Consequence
  • intron variant
See all consequences
HGVS.g name
  • (GRCm39)11:69689200C>T
HGVS.c name
  • ENSEMBL:ENSMUST00000011285.1:c.524-102G>A
  • ENSEMBL:ENSMUST00000102585.1:c.608-102G>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

Sequence feature
Sequence feature type
Associated gene
Location
Molecular consequence
Codon and amino acid change
ENSEMBL:ENSMUST00000011285
protein_codingFgf11Intron 4/5
  • intron variant
ENSEMBL:ENSMUST00000102585
protein_codingFgf11Intron 4/4
  • intron variant
RefSeq:NM_001291104.2
protein_codingFgf11Intron 4/5
  • intron variant
RefSeq:NM_001362623.1
protein_codingFgf11Intron 4/4
  • intron variant
RefSeq:NM_001362624.1
protein_codingFgf11Intron 4/4
  • intron variant
RefSeq:NM_010198.3
protein_codingFgf11Intron 4/5
  • intron variant
RefSeq:XM_006532188.5
protein_codingFgf11Intron 4/4
  • intron variant
RefSeq:XM_011248721.3
protein_codingFgf11Intron 4/4
  • intron variant
RefSeq:XM_011248722.3
protein_codingFgf11Intron 4/5
  • intron variant
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