Product Details

SNP ID
rs2000882
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.9:36836811 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GGGAAGTGGGGGACAGCACATGACC[C/T]TGGCACCTGGACCCCTGGAGTCAGG
Phenotype
MIM: 167414
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
PAX5 PubMed Links

Gene Details

Gene
PAX5
Gene Name
paired box 5
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001280547.1 5184 UTR 3 NP_001267476.1
NM_001280548.1 5184 UTR 3 NP_001267477.1
NM_001280549.1 5184 UTR 3 NP_001267478.1
NM_001280550.1 5184 UTR 3 NP_001267479.1
NM_001280551.1 5184 UTR 3 NP_001267480.1
NM_001280552.1 5184 UTR 3 NP_001267481.1
NM_001280553.1 5184 UTR 3 NP_001267482.1
NM_001280554.1 5184 UTR 3 NP_001267483.1
NM_001280555.1 5184 UTR 3 NP_001267484.1
NM_001280556.1 5184 UTR 3 NP_001267485.1
NM_016734.2 5184 UTR 3 NP_057953.1
XM_005251481.4 5184 UTR 3 XP_005251538.1
XM_011517896.2 5184 UTR 3 XP_011516198.1
XM_011517897.2 5184 UTR 3 XP_011516199.1

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