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TGCATTTTGCTGTTGTTGGATGGAA[C/T]ATTCTATGTGTCAATTAGATGAAGT
Species: |
Human | |||||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 616031 | |||||||||||||||||||||||||||||||||||||||||
Literature Links: |
CCDC141 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)
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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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CCDC141 - coiled-coil domain containing 141 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001316745.1 | Intron | NP_001303674.1 | ||||
NM_173648.3 | Intron | NP_775919.3 | ||||
XM_011510991.2 | Intron | XP_011509293.1 | ||||
XM_011510992.2 | Intron | XP_011509294.1 | ||||
XM_011510993.2 | Intron | XP_011509295.1 | ||||
XM_017003867.1 | Intron | XP_016859356.1 | ||||
XM_017003868.1 | Intron | XP_016859357.1 | ||||
XM_017003869.1 | Intron | XP_016859358.1 | ||||
XM_017003870.1 | Intron | XP_016859359.1 | ||||
XM_017003871.1 | Intron | XP_016859360.1 |