Product Details

SNP ID
rs2839369
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.21:46635536 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CCAGCTGCAGACGATCTGTGAGCGA[C/G]GCGCCGGCGCAAGTCGAGGGCGGTG
Phenotype
MIM: 601961
Polymorphism
C/G, Transversion substitution
Allele Nomenclature
Literature Links
PRMT2 PubMed Links

Gene Details

Gene
PRMT2
Gene Name
protein arginine methyltransferase 2
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001242864.2 384 Intron NP_001229793.1
NM_001242865.2 384 Intron NP_001229794.1
NM_001242866.2 384 Intron NP_001229795.1
NM_001286676.1 384 Intron NP_001273605.1
NM_001286677.1 384 Intron NP_001273606.1
NM_001286678.1 384 Intron NP_001273607.1
NM_001535.4 384 Intron NP_001526.2
NM_206962.3 384 Intron NP_996845.1
XM_005261111.3 384 UTR 5 XP_005261168.1
XM_006723998.3 384 Intron XP_006724061.1
XM_006723999.2 384 Intron XP_006724062.1
XM_006724000.2 384 Intron XP_006724063.1
XM_017028339.1 384 Intron XP_016883828.1
XM_017028340.1 384 UTR 5 XP_016883829.1

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