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rs108876629 SNP Detail
Summary
  • ID
    rs108876629
  • Variation Type
    SNP
  • Alleles
    A/G
Genome Location and Flanking Sequence
  • Location
    Chr15:64155540 (GRCm39)
  • SNP Orientation to the Genome
    forward
  • SNP Reference Flanking Sequence
                                                TGGGGTATTC CTGACAGTAT
    GAAGACCCAC TTCTATTTCT AACCTTACAT TTTTTTCTTT TATTTTTCTG AAATTATGTG
    CCCAGAATGG GCTATCGCCT CATTTAGACC TGGGTTTAAG ACCTTCCCGT ACACATAAAG
    GTTTCTAGTG CACAGTTCCC CTGCTGCTGA ACAGGGCTAG TACGTCCCAA GTGCAGGCAG
    R
    ACAGAACCTA GCAGGCACAC ATGAAATGGC AACTAGTCTT AAGTCTCAGG ACTTACAGGA
    GGCTGCCTGC AGAGGAAGAA TACTACCGCT GCGCTATCCT GATTCACCTG TCACCTTGGT
    CAGTGTTGCT TCCTCTTTCC TTGGCAGCAG CTGAAGAAAA TGGGTCCAGA GCACTAAGTA
    GTCACAAAGC TCGCTAGCTC                                            
    
    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
A/J
DBA/2J
MSM/Ms
ss148017152 ENSMUSSNP3177578 ENSEMBL ENSEMBL_Sanger f SNP A A G
SNP Consensus Information
SNP Consensus Type
A/J
DBA/2J
MSM/Ms
rs108876629 SNP A A G
Gene/Marker
Associations
and
Function
Classes
MGI genes/markers associated with the SNP
Location: Chr15:64155540 () rs orientation: forward
Symbol Name Transcript Protein Function
Class
Allele Residue Codon
Position
AA
Position
Asap1 ArfGAP with SH3 domain, ankyrin repeat and PH domain1 Intron
Noncoding-Transcript-Variant
Rr503380 regulatory region 503380 1504 bp proximal
Tssr134529 transcription start site region 134529 1597 bp downstream

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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last database update
03/18/2025
MGI 6.24
The Jackson Laboratory