Product Details

SNP ID
hCV26501719
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.7:130506500 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
AGAATAAAAAGAAAAAAAAAAAAAA[A/C]CAACCCATGCGCAAAGATAGACATT
Phenotype
MIM: 604355 MIM: 601029
Polymorphism
A/C, Transversion substitution
Allele Nomenclature
Literature Links
COPG2 PubMed Links

Gene Details

Gene
COPG2
Gene Name
coatomer protein complex subunit gamma 2
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001290033.1 2882 Intron NP_001276962.1
NM_012133.5 2882 UTR 3 NP_036265.3
Gene
MEST
Gene Name
mesoderm specific transcript
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001253900.1 2882 Intron NP_001240829.1
NM_001253901.1 2882 Intron NP_001240830.1
NM_001253902.1 2882 Intron NP_001240831.1
NM_002402.3 2882 Intron NP_002393.2
NM_177524.2 2882 Intron NP_803490.1
NM_177525.2 2882 Intron NP_803491.1

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