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CTACTGTCTTATTAGAAGGATAAAA[A/C]ACTTTGAATGAAAATCCACTTCTTG
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 602670 | ||||||||||||||||||||
Literature Links: |
POLE2 PubMed Links | ||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap |
---|---|---|
Global - Not Available | Caucasian - Not Available | CEPH (CEU) - Not Available |
EAS - Not Available | African American - Not Available | YRI (Yoruba) - Not Available |
SAS - Not Available | Chinese - Not Available | CHB (Han Chinese) - Not Available |
AFR - Not Available | Japanese - Not Available | JPT (Japanese) - Not Available |
EUR - Not Available | ||
AMR - Not Available |
POLE2 - DNA polymerase epsilon 2, accessory subunit | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001197330.1 | 1710 | Silent Mutation | GTG,GTT | V,V 485 | NP_001184259.1 | |
NM_001197331.1 | 1710 | Intron | NP_001184260.1 | |||
NM_002692.3 | 1710 | Silent Mutation | GTG,GTT | V,V 511 | NP_002683.2 | |
XM_011536842.2 | 1710 | Silent Mutation | GTG,GTT | V,V 485 | XP_011535144.1 | |
XM_011536843.2 | 1710 | Silent Mutation | GTG,GTT | V,V 434 | XP_011535145.1 | |
XM_011536844.1 | 1710 | Intron | XP_011535146.1 | |||
XM_017021374.1 | 1710 | Silent Mutation | GTG,GTT | V,V 511 | XP_016876863.1 | |
XM_017021375.1 | 1710 | Silent Mutation | GTG,GTT | V,V 434 | XP_016876864.1 |