Product Details

SNP ID
rs10733253
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.9:13105639 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
CATGATAAAAACCAATTTTAAGTTG[C/T]AAATCTTGAACAGTATATAACAAAG
Phenotype
MIM: 603785
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
MPDZ PubMed Links

Gene Details

Gene
MPDZ
Gene Name
multiple PDZ domain crumbs cell polarity complex component
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001261406.1 7710 Intron NP_001248335.1
NM_001261407.1 7710 Intron NP_001248336.1
NM_003829.4 7710 Intron NP_003820.2
XM_005251622.4 7710 UTR 3 XP_005251679.1
XM_005251623.4 7710 Intron XP_005251680.1
XM_006716885.3 7710 Intron XP_006716948.1
XM_006716886.3 7710 Intron XP_006716949.1
XM_006716887.3 7710 Intron XP_006716950.1
XM_006716888.3 7710 Intron XP_006716951.1
XM_006716889.3 7710 Intron XP_006716952.1
XM_006716891.3 7710 Intron XP_006716954.1
XM_017015252.1 7710 Intron XP_016870741.1
XM_017015253.1 7710 Intron XP_016870742.1
XM_017015254.1 7710 Intron XP_016870743.1
XM_017015255.1 7710 Intron XP_016870744.1
XM_017015256.1 7710 Intron XP_016870745.1
XM_017015257.1 7710 Intron XP_016870746.1
XM_017015258.1 7710 Intron XP_016870747.1
XM_017015259.1 7710 Intron XP_016870748.1

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