Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
GCGCGGTTCTGGTGGGCATGTCTTC[C/G]AAGAGCGATGCGAGTGTCAGTGGTT
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 604355 | ||||||||||||||||||||
Literature Links: |
COPG2 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 |
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 | 1584 | Intron | NP_001276962.1 | |||
NM_012133.5 | 1584 | Intron | NP_036265.3 |
TSGA13 - testis specific 13 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001304968.1 | 1584 | Missense Mutation | TTC,TTG | F,L 244 | NP_001291897.1 | |
NM_052933.3 | 1584 | Missense Mutation | TTC,TTG | F,L 244 | NP_443165.1 |