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GTTTTCATGTAGGATCATTTCCCTT[A/C]AACCTGACAACTTTATGTTTATATT
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 601961 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
PRMT2 PubMed Links | ||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
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Global
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Caucasian - Not Available | CEPH (CEU) - Not Available | |||
EAS
|
African American - Not Available | YRI (Yoruba) - Not Available | |||
SAS
|
Chinese - Not Available | CHB (Han Chinese) - Not Available | |||
AFR
|
Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR
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AMR
|
PRMT2 - protein arginine methyltransferase 2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001242864.2 | Intron | NP_001229793.1 | ||||
NM_001242865.2 | Intron | NP_001229794.1 | ||||
NM_001242866.2 | Intron | NP_001229795.1 | ||||
NM_001286676.1 | Intron | NP_001273605.1 | ||||
NM_001286677.1 | Intron | NP_001273606.1 | ||||
NM_001286678.1 | Intron | NP_001273607.1 | ||||
NM_001535.4 | Intron | NP_001526.2 | ||||
NM_206962.3 | Intron | NP_996845.1 | ||||
XM_005261111.3 | Intron | XP_005261168.1 | ||||
XM_006723998.3 | Intron | XP_006724061.1 | ||||
XM_006723999.2 | Intron | XP_006724062.1 | ||||
XM_006724000.2 | Intron | XP_006724063.1 | ||||
XM_017028339.1 | Intron | XP_016883828.1 | ||||
XM_017028340.1 | Intron | XP_016883829.1 |