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AAAATACAGGTTTCTTGGATACTGA[C/G]CAGAAACAACTGCGATACAGTAGTC
Species: |
Human | ||||||||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
15 submissions
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Phenotype: |
MIM: 614695 | ||||||||||||||||||||||||||||||||||||||||||||
Literature Links: |
RPRD2 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)
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EAS
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African American - Not Available | YRI (Yoruba) - Not Available | ||||||
SAS
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Chinese - Not Available | CHB (Han Chinese) - Not Available | ||||||
AFR
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Japanese - Not Available | JPT (Japanese)
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EUR
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AMR
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RPRD2 - regulation of nuclear pre-mRNA domain containing 2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001297673.1 | Intron | NP_001284602.1 | ||||
NM_001297674.1 | Intron | NP_001284603.1 | ||||
NM_015203.4 | Intron | NP_056018.2 | ||||
XM_005245033.2 | Intron | XP_005245090.1 | ||||
XM_006711240.2 | Intron | XP_006711303.1 | ||||
XM_011509344.2 | Intron | XP_011507646.1 | ||||
XM_017000763.1 | Intron | XP_016856252.1 | ||||
XM_017000764.1 | Intron | XP_016856253.1 | ||||
XM_017000765.1 | Intron | XP_016856254.1 | ||||
XM_017000766.1 | Intron | XP_016856255.1 | ||||
XM_017000767.1 | Intron | XP_016856256.1 |
Set Membership: |
HapMap |