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rs47498502 SNP Detail
Summary
  • ID
    rs47498502
  • Variation Type
    SNP
  • Alleles
    C/T
Genome Location and Flanking Sequence
  • Location
    Chr6:88365658 (GRCm39)
  • SNP Orientation to the Genome
    forward
  • SNP Reference Flanking Sequence
                                                CATTTTTTTG GATGGAGACT
    GGGGACTGAA GAGGCACCGC AGGCCTCATT TCAGAAGGGG CAGCAGGAAC ACATCTCACT
    GTGAAGGGCT GCAGAGTCCA CAATGTCCTG TGGGCCCAAC AGTTAGCAAC TTAGGGATGA
    AATCAATGAG AGGCCTGCCA GGACACAGAG GCCCCTGGAG GAAGTGGTAG GCAGGACAGG
    Y
    CAGTGTGTCA GGGAAACATC TCCATCGAGG CTCTCCTCCC CACTGTTCAT CTCCAAGATG
    CCCCACCCTA ATACCTGCAA ACTAGCTACC CAAGTTCCAC CTGGTACCAG GCACTGAAAT
    GAGTCTGGTC CTCTCCCATC TGAACACCTG TTCAGGTATT CCATGGATAG AACTCCAGGA
    CTCAGGAGTC CAACACTGTT                                            
    
    Y = C/T
    

    Note: Sequence in lower case indicates low-complexity or repetitive sequence
    BLAST SNP flanking sequence against the mouse Genome
SNP Assays
and
SNP Consensus
Strain alleles of submitted assays, and consensus values for this SNP
Legend
Assay ID Submitter
SNP ID
Submitter
Handle
Population
ss orientation
Variation Type
A/J
DBA/2J
MSM/Ms
ss133364918 ENSMUSSNP2032187 ENSEMBL ENSEMBL_Sanger f SNP T T C
SNP Consensus Information
SNP Consensus Type
A/J
DBA/2J
MSM/Ms
rs47498502 SNP T T C
Gene/Marker
Associations
and
Function
Classes
MGI genes/markers associated with the SNP
Location: Chr6:88365658 () rs orientation: forward
Symbol Name Transcript Protein Function
Class
Allele Residue Codon
Position
AA
Position
Eefsec eukaryotic elongation factor, selenocysteine-tRNA-specific Intron
Noncoding-Transcript-Variant
Rr633881 regulatory region 633881 within coordinates
Rr633882 regulatory region 633882 307 bp proximal

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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Funding Information
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last database update
03/25/2025
MGI 6.24
The Jackson Laboratory