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CCCAGCCATGTCCTCTGCATGCATC[A/G]CTGTGTCCTTGTGAACAGTGGATCT
Species: |
Human | ||||||||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 607929 | ||||||||||||||||||||||||||||||||||||||||||||
Literature Links: |
CCM2 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)
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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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CCM2 - CCM2 scaffolding protein | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001029835.2 | Intron | NP_001025006.1 | ||||
NM_001167934.1 | Intron | NP_001161406.1 | ||||
NM_001167935.1 | Intron | NP_001161407.1 | ||||
NM_031443.3 | Intron | NP_113631.1 | ||||
XM_006715785.3 | Intron | XP_006715848.1 | ||||
XM_006715786.3 | Intron | XP_006715849.1 | ||||
XM_011515561.2 | Intron | XP_011513863.1 | ||||
XM_011515562.1 | Intron | XP_011513864.1 | ||||
XM_011515563.2 | Intron | XP_011513865.1 | ||||
XM_011515564.2 | Intron | XP_011513866.1 | ||||
XM_017012671.1 | Intron | XP_016868160.1 | ||||
XM_017012672.1 | Intron | XP_016868161.1 | ||||
XM_017012673.1 | Intron | XP_016868162.1 |