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ATTTGGGTTTTGGAAAAATCGTTAT[C/T]ATCTACTTTGGGATACAATTGGCTC
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
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Literature Links: |
CCDC102B 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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CCDC102B - coiled-coil domain containing 102B | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001093729.1 | Intron | NP_001087198.1 | ||||
NM_024781.2 | Intron | NP_079057.2 | ||||
XM_011526174.2 | Intron | XP_011524476.1 | ||||
XM_011526175.2 | Intron | XP_011524477.1 | ||||
XM_017025973.1 | Intron | XP_016881462.1 | ||||
XM_017025974.1 | Intron | XP_016881463.1 | ||||
XM_017025975.1 | Intron | XP_016881464.1 | ||||
XM_017025976.1 | Intron | XP_016881465.1 | ||||
XM_017025977.1 | Intron | XP_016881466.1 | ||||
XM_017025978.1 | Intron | XP_016881467.1 | ||||
XM_017025979.1 | Intron | XP_016881468.1 | ||||
XM_017025980.1 | Intron | XP_016881469.1 |