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CCTCGTTGGATCGAAAATTCCAGTC[G/T]GTAACCAACACCATGGAGTCCATTC
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
22 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) - Not Available | |||
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) - Not Available | |||
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 | 378 | Silent Mutation | TCG,TCT | S,S 33 | NP_001284602.1 | |
NM_001297674.1 | 378 | Silent Mutation | TCG,TCT | S,S 33 | NP_001284603.1 | |
NM_015203.4 | 378 | Silent Mutation | TCG,TCT | S,S 33 | NP_056018.2 | |
XM_005245033.2 | 378 | Silent Mutation | TCG,TCT | S,S 33 | XP_005245090.1 | |
XM_006711240.2 | 378 | Silent Mutation | TCG,TCT | S,S 33 | XP_006711303.1 | |
XM_011509344.2 | 378 | Silent Mutation | TCG,TCT | S,S 33 | XP_011507646.1 | |
XM_017000763.1 | 378 | Silent Mutation | TCG,TCT | S,S 33 | XP_016856252.1 | |
XM_017000764.1 | 378 | Intron | XP_016856253.1 | |||
XM_017000765.1 | 378 | Silent Mutation | TCG,TCT | S,S 33 | XP_016856254.1 | |
XM_017000766.1 | 378 | Silent Mutation | TCG,TCT | S,S 33 | XP_016856255.1 | |
XM_017000767.1 | 378 | Silent Mutation | TCG,TCT | S,S 33 | XP_016856256.1 |