Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
CTTGCCGGTGCAGCTCTCGGAGAAC[A/G]TCTAATATTGAGTCTAGTTCTGTGC
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 610201 MIM: 615410 | ||||||||||||||||||||
Literature Links: |
CEP162 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 |
CEP162 - centrosomal protein 162 | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001286206.1 | 4372 | Silent Mutation | GAC,GAT | D,D 1302 | NP_001273135.1 | |
NM_014895.3 | 4372 | Silent Mutation | GAC,GAT | D,D 1378 | NP_055710.2 | |
XM_005248674.3 | 4372 | Silent Mutation | GAC,GAT | D,D 1340 | XP_005248731.1 | |
XM_005248678.3 | 4372 | Intron | XP_005248735.1 | |||
XM_006715380.2 | 4372 | Silent Mutation | GAC,GAT | D,D 1302 | XP_006715443.1 | |
XM_011535592.2 | 4372 | Silent Mutation | GAC,GAT | D,D 989 | XP_011533894.1 | |
XM_011535594.2 | 4372 | Intron | XP_011533896.1 | |||
XM_017010483.1 | 4372 | Silent Mutation | GAC,GAT | D,D 1340 | XP_016865972.1 | |
XM_017010484.1 | 4372 | Silent Mutation | GAC,GAT | D,D 1302 | XP_016865973.1 |
MRAP2 - melanocortin 2 receptor accessory protein 2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_138409.2 | 4372 | Intron | NP_612418.2 | |||
XM_011535400.2 | 4372 | Intron | XP_011533702.1 | |||
XM_017010219.1 | 4372 | Intron | XP_016865708.1 | |||
XM_017010220.1 | 4372 | Intron | XP_016865709.1 | |||
XM_017010221.1 | 4372 | Intron | XP_016865710.1 |