Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
CTCCAAGGCTGTCAGGAAGCACTCC[A/G]TAGCCGCCGCATCGTTGCCCTGAGC
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
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Literature Links: |
TTC7B 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 |
TTC7B - tetratricopeptide repeat domain 7B | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001010854.1 | 2099 | Missense Mutation | ACG,ATG | T,M 818 | NP_001010854.1 | |
NM_001320421.1 | 2099 | Missense Mutation | ACG,ATG | T,M 733 | NP_001307350.1 | |
XM_005267367.1 | 2099 | Missense Mutation | ACG,ATG | T,M 631 | XP_005267424.1 | |
XM_011536497.1 | 2099 | Missense Mutation | ACG,ATG | T,M 787 | XP_011534799.1 | |
XM_017021044.1 | 2099 | Missense Mutation | ACG,ATG | T,M 889 | XP_016876533.1 | |
XM_017021045.1 | 2099 | Missense Mutation | ACG,ATG | T,M 835 | XP_016876534.1 | |
XM_017021046.1 | 2099 | Missense Mutation | ACG,ATG | T,M 716 | XP_016876535.1 | |
XM_017021047.1 | 2099 | Missense Mutation | ACG,ATG | T,M 560 | XP_016876536.1 |