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TTTTGCAGGATCTTGTTCAAGATGG[A/G]GTGGCTTCACCAGCTACCCCTGGGA
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 612711 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
GCC2 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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GCC2 - GRIP and coiled-coil domain containing 2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_181453.3 | 178 | Silent Mutation | GGA,GGG | G,G 8 | NP_852118.1 | |
XM_006712870.3 | 178 | Silent Mutation | GGA,GGG | G,G 11 | XP_006712933.1 | |
XM_006712871.1 | 178 | UTR 5 | XP_006712934.1 | |||
XM_006712872.3 | 178 | Silent Mutation | GGA,GGG | G,G 11 | XP_006712935.1 | |
XM_011512213.2 | 178 | Intron | XP_011510515.1 |