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TGGTCACTCCATCGGCTAAGGCCAG[C/T]CTGGACCTCACCAATAAATCATAGC
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 604355 MIM: 601029 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
COPG2 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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COPG2 - coatomer protein complex subunit gamma 2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001290033.1 | 2616 | Intron | NP_001276962.1 | |||
NM_012133.5 | 2616 | Silent Mutation | AGA,AGG | R,R 842 | NP_036265.3 |
MEST - mesoderm specific transcript | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001253900.1 | 2616 | Intron | NP_001240829.1 | |||
NM_001253901.1 | 2616 | Intron | NP_001240830.1 | |||
NM_001253902.1 | 2616 | Intron | NP_001240831.1 | |||
NM_002402.3 | 2616 | Intron | NP_002393.2 | |||
NM_177524.2 | 2616 | Intron | NP_803490.1 | |||
NM_177525.2 | 2616 | Intron | NP_803491.1 | |||
XM_011516222.1 | 2616 | Intron | XP_011514524.1 | |||
XM_017012218.1 | 2616 | Intron | XP_016867707.1 |