Product Details

SNP ID
rs145873765
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.14:90541447 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CTCCAAGGCTGTCAGGAAGCACTCC[A/G]TAGCCGCCGCATCGTTGCCCTGAGC
Phenotype
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
TTC7B PubMed Links

Gene Details

Gene
TTC7B
Gene Name
tetratricopeptide repeat domain 7B
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001010854.1 2099 Missense Mutation ACG,ATG T818M NP_001010854.1
NM_001320421.1 2099 Missense Mutation ACG,ATG T733M NP_001307350.1
XM_005267367.1 2099 Missense Mutation ACG,ATG T631M XP_005267424.1
XM_011536497.1 2099 Missense Mutation ACG,ATG T787M XP_011534799.1
XM_017021044.1 2099 Missense Mutation ACG,ATG T889M XP_016876533.1
XM_017021045.1 2099 Missense Mutation ACG,ATG T835M XP_016876534.1
XM_017021046.1 2099 Missense Mutation ACG,ATG T716M XP_016876535.1
XM_017021047.1 2099 Missense Mutation ACG,ATG T560M XP_016876536.1

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