Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
Species: |
Human | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 601053 MIM: 615808 | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Literature Links: |
CCDC51 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
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CEPH (CEU)
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EAS
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African American
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YRI (Yoruba)
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SAS
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Japanese
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JPT (Japanese)
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AFR
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Chinese
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CHB (Han Chinese)
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EUR
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AMR
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CCDC51 - coiled-coil domain containing 51 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001256964.1 | 1272 | Silent Mutation | CTG,TTG | L,L 269 | NP_001243893.1 | |
NM_001256965.2 | 1272 | Silent Mutation | CTG,TTG | L,L 160 | NP_001243894.1 | |
NM_001256966.2 | 1272 | Silent Mutation | CTG,TTG | L,L 160 | NP_001243895.1 | |
NM_001256967.2 | 1272 | Silent Mutation | CTG,TTG | L,L 160 | NP_001243896.1 | |
NM_001256968.2 | 1272 | Silent Mutation | CTG,TTG | L,L 160 | NP_001243897.1 | |
NM_001256969.2 | 1272 | Silent Mutation | CTG,TTG | L,L 160 | NP_001243898.1 | |
NM_024661.4 | 1272 | Silent Mutation | CTG,TTG | L,L 269 | NP_078937.3 | |
XM_011534113.2 | 1272 | Silent Mutation | CTG,TTG | L,L 289 | XP_011532415.1 |
PLXNB1 - plexin B1 | ||||||
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There are no transcripts associated with this gene. |
TMA7 - translation machinery associated 7 homolog | ||||||
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There are no transcripts associated with this gene. |