Product Details

SNP ID
rs189421291
Assay Type
Functionally tested
NCBI dbSNP Submissions
6
Location
Chr.1:54782444 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
ATGCCCCCGAGACCCATCTTGGCCC[A/G]CTTGAGGTCATGCAGGTAGGCTCTG
Phenotype
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
TTC22 PubMed Links

Gene Details

Gene
TTC22
Gene Name
tetratricopeptide repeat domain 22
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001114108.1 1159 Missense Mutation CGG,TGG R352W NP_001107580.1
NM_017904.3 1159 Intron NP_060374.2
XM_011541671.2 1159 Intron XP_011539973.1
XM_017001582.1 1159 Missense Mutation CGG,TGG R161W XP_016857071.1

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