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ACCTGCCAAGAGCCAGAGAGCATCC[C/T]TGTCAGAGCCTCCCTGCAGTTCCCA
Species: |
Human | |||||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
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Literature Links: |
CCDC157 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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CCDC157 - coiled-coil domain containing 157 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001017437.3 | 895 | Missense Mutation | CCT,CTT | P,L 191 | NP_001017437.2 | |
NM_001318334.1 | 895 | Missense Mutation | CCT,CTT | P,L 191 | NP_001305263.1 | |
NM_001318335.1 | 895 | Intron | NP_001305264.1 | |||
XM_006724278.3 | 895 | Missense Mutation | CCT,CTT | P,L 191 | XP_006724341.1 | |
XM_006724279.3 | 895 | Missense Mutation | CCT,CTT | P,L 191 | XP_006724342.1 | |
XM_006724280.3 | 895 | Missense Mutation | CCT,CTT | P,L 191 | XP_006724343.1 | |
XM_011530263.2 | 895 | Missense Mutation | CCT,CTT | P,L 191 | XP_011528565.1 | |
XM_011530266.2 | 895 | Missense Mutation | CCT,CTT | P,L 191 | XP_011528568.1 | |
XM_011530267.2 | 895 | Missense Mutation | CCT,CTT | P,L 191 | XP_011528569.1 | |
XM_011530268.2 | 895 | Missense Mutation | CCT,CTT | P,L 191 | XP_011528570.1 | |
XM_011530269.2 | 895 | Intron | XP_011528571.1 | |||
XM_011530270.2 | 895 | Missense Mutation | CCT,CTT | P,L 191 | XP_011528572.1 |
KIAA1656 - KIAA1656 protein | ||||||
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There are no transcripts associated with this gene. |
RNF215 - ring finger protein 215 | ||||||
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There are no transcripts associated with this gene. |