Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
AATCTGAACAAAGTGAAAAACAGCC[C/T]TTTGAGTCTTTCTGATACCTGAGTT
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 612328 MIM: 609641 | ||||||||||||||||||||
Literature Links: |
CCDC73 PubMed Links | ||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap |
---|---|---|
Global - Not Available | Caucasian - Not Available | CEPH (CEU) - Not Available |
EAS - Not Available | African American - Not Available | YRI (Yoruba) - Not Available |
SAS - Not Available | Chinese - Not Available | CHB (Han Chinese) - Not Available |
AFR - Not Available | Japanese - Not Available | JPT (Japanese) - Not Available |
EUR - Not Available | ||
AMR - Not Available |
CCDC73 - coiled-coil domain containing 73 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001008391.3 | 828 | UTR 3 | NP_001008392.2 | |||
XM_011520139.2 | 828 | UTR 3 | XP_011518441.1 |
EIF3M - eukaryotic translation initiation factor 3 subunit M | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001307929.1 | 828 | Missense Mutation | CCT,CTT | P,L 236 | NP_001294858.1 | |
NM_006360.5 | 828 | Missense Mutation | CCT,CTT | P,L 368 | NP_006351.2 | |
XM_011519840.2 | 828 | Missense Mutation | CCT,CTT | P,L 305 | XP_011518142.1 |