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CGACTCTGCTTGGCTTTGGCGATGG[A/T]CTCCTCACTGCCGCCTGCTGGGGCC
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) - 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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CCM2 - CCM2 scaffolding protein | ||||||
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There are no transcripts associated with this gene. |
LOC100128364 - uncharacterized LOC100128364 | ||||||
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There are no transcripts associated with this gene. |
NACAD - NAC alpha domain containing | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001146334.1 | 4120 | Missense Mutation | ACC,TCC | T,S 1404 | NP_001139806.1 | |
XM_006715674.3 | 4120 | Missense Mutation | ACC,TCC | T,S 1191 | XP_006715737.1 |