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TGTGGGACTGGACTGTGGCCCCACC[C/T]GTCCCAGCCACCCCCTATGAAGCCT
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 174761 MIM: 606802 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
POLD1 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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POLD1 - DAN polymerase delta 1, catalytic subunit | ||||||
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There are no transcripts associated with this gene. |
SPIB - Spi-B transcription factor | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001243998.1 | 181 | Intron | NP_001230927.1 | |||
NM_001243999.1 | 181 | Silent Mutation | CCC,CCT | P,P 52 | NP_001230928.1 | |
NM_001244000.1 | 181 | Missense Mutation | CCG,CTG | P,L 33 | NP_001230929.1 | |
NM_003121.4 | 181 | Silent Mutation | CCC,CCT | P,P 52 | NP_003112.2 |