Product Details

SNP ID
rs41269795
Assay Type
Functionally Tested
NCBI dbSNP Submissions
11
Location
Chr.1:13704975 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
AAAGTAGGAGTTTTCAGAAGTATGG[C/T]TCTTGGGATAAATTTAGATTCTTAA
Phenotype
MIM: 601196
Polymorphism
C/T, Transition Substitution
Allele Nomenclature
Literature Links
PRDM2 PubMed Links

Gene Details

Gene
PRDM2
Gene Name
PR domain 2
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001007257.2 121 Intron NP_001007258.1
NM_001135610.1 121 Intron NP_001129082.1
NM_012231.4 121 UTR 5 NP_036363.2
NM_015866.4 121 UTR 5 NP_056950.2
XM_017002253.1 121 Intron XP_016857742.1
XM_017002254.1 121 Intron XP_016857743.1
XM_017002255.1 121 Intron XP_016857744.1
XM_017002256.1 121 Intron XP_016857745.1
XM_017002257.1 121 Intron XP_016857746.1
XM_017002258.1 121 Intron XP_016857747.1
XM_017002259.1 121 Intron XP_016857748.1
XM_017002260.1 121 Intron XP_016857749.1
XM_017002261.1 121 Intron XP_016857750.1
XM_017002262.1 121 Intron XP_016857751.1
XM_017002263.1 121 Intron XP_016857752.1
XM_017002264.1 121 Intron XP_016857753.1

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