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TGGCGAGGACCGCGCACATTCTGAC[C/G]GATCGCTGCGGGCAGGAGGCGGTGA
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 600637 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
CCDC105 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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CCDC105 - coiled-coil domain containing 105 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_173482.2 | 207 | Silent Mutation | ACC,ACG | T,T 36 | NP_775753.2 |
SLC1A6 - solute carrier family 1 member 6 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001272087.1 | 207 | Intron | NP_001259016.1 | |||
NM_001272088.1 | 207 | Intron | NP_001259017.1 | |||
NM_005071.2 | 207 | Intron | NP_005062.1 | |||
XM_006722842.1 | 207 | Intron | XP_006722905.1 | |||
XM_006722844.1 | 207 | Intron | XP_006722907.1 | |||
XM_017027152.1 | 207 | Intron | XP_016882641.1 |