Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
AGTGAGATGGAAGATTTTCGAGGTA[G/T]AGCAGAAGAATCATTTCCAAGCTTT
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 616426 | ||||||||||||||||||||
Literature Links: |
CEP192 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 |
CEP192 - centrosomal protein 192 | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_032142.3 | 155 | Missense Mutation | AGA,ATA | R,I 7 | NP_115518.3 | |
XM_005258107.3 | 155 | Missense Mutation | AGA,ATA | R,I 7 | XP_005258164.1 | |
XM_005258109.3 | 155 | Missense Mutation | AGA,ATA | R,I 7 | XP_005258166.1 | |
XM_005258110.1 | 155 | Intron | XP_005258167.1 | |||
XM_006722326.3 | 155 | Missense Mutation | AGA,ATA | R,I 7 | XP_006722389.1 | |
XM_006722327.3 | 155 | Missense Mutation | AGA,ATA | R,I 7 | XP_006722390.1 | |
XM_006722330.3 | 155 | Missense Mutation | AGA,ATA | R,I 7 | XP_006722393.1 | |
XM_011525673.2 | 155 | Missense Mutation | AGA,ATA | R,I 7 | XP_011523975.1 | |
XM_011525675.2 | 155 | Intron | XP_011523977.1 | |||
XM_017025803.1 | 155 | UTR 5 | XP_016881292.1 | |||
XM_017025804.1 | 155 | Missense Mutation | AGA,ATA | R,I 7 | XP_016881293.1 | |
XM_017025805.1 | 155 | Intron | XP_016881294.1 | |||
XM_017025806.1 | 155 | Intron | XP_016881295.1 | |||
XM_017025807.1 | 155 | Intron | XP_016881296.1 |