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CCTCACTGGGAATGTCATCATTACC[A/C]ACTTCAGATGGGTTTAACCATCCCG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
14 submissions
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Phenotype: |
MIM: 601966 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
DDI2 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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DDI2 - DNA damage inducible 1 homolog 2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_032341.4 | 171 | UTR 3 | NP_115717.3 |
RSC1A1 - regulatory solute carrier protein, family 1, member 1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_006511.2 | 171 | Silent Mutation | CCA,CCC | P,P 5 | NP_006502.1 |