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rs27365958 SNP Detail
Summary
  • ID
    rs27365958
  • Variation Type
    SNP
  • Alleles
    A/G
Genome Location and Flanking Sequence
  • Location
    Chr2:154301402 (GRCm39)
  • SNP Orientation to the Genome
    forward
  • SNP Reference Flanking Sequence
                          ACCTTACATT CATATTTACT TGATTTTAAA GCAATTTTTG
    CATTGTCTTC TTATCTTTGA TTTACAGCCG CACCAGAACC GTTGTTGCCT GCATTGTCTT
    R
    ATTTAATCAT GGGCCAGTTT AGTAGAGCAC CAAGTCTGGA TCTGGGAGGC AGCTTGTGTG
    AATCATTTAC ATATATTTCT GCTTATGTTC CCAAAACTA                       
    
    R = A/G
    

    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
129S1/SvImJ
BTBR T<+> Itpr3/J
KK/HlJ
NZW/LacJ
ss37555781 NES08917293 PERLEGEN MM_PANEL2 f SNP A G G G
SNP Consensus Information
SNP Consensus Type
129S1/SvImJ
BTBR T<+> Itpr3/J
KK/HlJ
NZW/LacJ
rs27365958 SNP A G G G
Additional submitted assays for this SNP, where the strain of origin for observed alleles is not specified by the submitter
Assay ID Submitter
SNP ID
Submitter
Handle
Population
ss orientation
Variation
Type
Alleles
ss37555781 NES08917293 PERLEGEN MM_PANEL f SNP A/G
Gene/Marker
Associations
and
Function
Classes
MGI genes/markers associated with the SNP
Location: Chr2:154301402 () rs orientation: forward
Symbol Name Transcript Protein Function
Class
Allele Residue Codon
Position
AA
Position
Cbfa2t2 CBFA2/RUNX1 translocation partner 2 Intron
Rr567835 regulatory region 567835 186 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