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TGGGTCTGCCTGTCTAATGGTACAC[A/G]TGTGTCCTGGGATCCACAGTTAAAG
Species: |
Human | |||||||||||||||||||||||
dbSNP Submissions: |
NA
|
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Phenotype: |
MIM: 614169 | |||||||||||||||||||||||
Literature Links: |
CCDC12 PubMed Links | |||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
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Global
|
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 |
CCDC12 - coiled-coil domain containing 12 | ||||||
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There are no transcripts associated with this gene. |
NBEAL2 - neurobeachin like 2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_015175.2 | Intron | NP_055990.1 | ||||
XM_006713072.3 | Intron | XP_006713135.1 | ||||
XM_011533533.2 | Intron | XP_011531835.1 | ||||
XM_017006010.1 | Intron | XP_016861499.1 | ||||
XM_017006011.1 | Intron | XP_016861500.1 | ||||
XM_017006012.1 | Intron | XP_016861501.1 | ||||
XM_017006013.1 | Intron | XP_016861502.1 | ||||
XM_017006014.1 | Intron | XP_016861503.1 | ||||
XM_017006015.1 | Intron | XP_016861504.1 | ||||
XM_017006016.1 | Intron | XP_016861505.1 | ||||
XM_017006017.1 | Intron | XP_016861506.1 |