Product Details

SNP ID
rs201291303
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.7:130669127 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
ATGTCTTCCAAGAGCGATGCGAGTG[G/T]CAGTGGTTCCCGAATCACTTTGGAA
Phenotype
MIM: 604355
Polymorphism
G/T, 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 1567 Intron NP_001276962.1
NM_012133.5 1567 Intron NP_036265.3
Gene
TSGA13
Gene Name
testis specific 13
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001304968.1 1567 Missense Mutation ACA,CCA T239P NP_001291897.1
NM_052933.3 1567 Missense Mutation ACA,CCA T239P NP_443165.1

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