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TGTAGACTGCTCTCTACGGCCCAGC[C/T]GCCCACTGGAGGTCGCTGCTGCACC
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
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Literature Links: |
CCDC142 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 |
CCDC142 - coiled-coil domain containing 142 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_032779.3 | 125 | Intron | NP_116168.3 |
TTC31 - tetratricopeptide repeat domain 31 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_022492.4 | 125 | Missense Mutation | CGC,TGC | R,C 21 | NP_071937.4 | |
XM_005264492.1 | 125 | Missense Mutation | CGC,TGC | R,C 21 | XP_005264549.1 | |
XM_011533035.1 | 125 | Missense Mutation | CGC,TGC | R,C 21 | XP_011531337.1 | |
XM_011533036.1 | 125 | Missense Mutation | CGC,TGC | R,C 21 | XP_011531338.1 | |
XM_011533037.1 | 125 | Missense Mutation | CGC,TGC | R,C 21 | XP_011531339.1 | |
XM_011533040.1 | 125 | UTR 5 | XP_011531342.1 | |||
XM_017004706.1 | 125 | Missense Mutation | CGC,TGC | R,C 21 | XP_016860195.1 | |
XM_017004707.1 | 125 | Missense Mutation | CGC,TGC | R,C 21 | XP_016860196.1 | |
XM_017004708.1 | 125 | UTR 5 | XP_016860197.1 | |||
XM_017004709.1 | 125 | Intron | XP_016860198.1 |