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TGAATAGTACTAAGGCCTGTCCCCT[C/T]ACTGGTGACCCATCTTCCCAAGAGA
Species: |
Human | |||||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 612013 | |||||||||||||||||||||||||||||||||||||||||
Literature Links: |
CC2D2A 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)
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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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CC2D2A - coiled-coil and C2 domain containing 2A | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001080522.2 | Intron | NP_001073991.2 | ||||
NM_001164720.1 | Intron | NP_001158192.1 | ||||
NM_020785.2 | Intron | NP_065836.2 | ||||
XM_005248177.1 | Intron | XP_005248234.1 | ||||
XM_011513872.2 | Intron | XP_011512174.1 | ||||
XM_011513874.2 | Intron | XP_011512176.1 | ||||
XM_017008482.1 | Intron | XP_016863971.1 |