Product Details

SNP ID
rs182221685
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.7:101316486 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CCGGTGGCTTGGGATGTCAGCATTG[A/C]AGACGATCACCACTCCATGAGCATC
Phenotype
Polymorphism
A/C, Transversion substitution
Allele Nomenclature
Literature Links
IFT22 PubMed Links

Gene Details

Gene
IFT22
Gene Name
intraflagellar transport 22
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001130820.2 450 Missense Mutation TGC,TTC C58F NP_001124292.1
NM_001130821.2 450 Missense Mutation TGC,TTC C11F NP_001124293.1
NM_001130822.2 450 Missense Mutation TGC,TTC C11F NP_001124294.1
NM_001287525.1 450 Missense Mutation TGC,TTC C11F NP_001274454.1
NM_001287526.1 450 Missense Mutation TGC,TTC C11F NP_001274455.1
NM_022777.3 450 Missense Mutation TGC,TTC C88F NP_073614.1
Gene
LOC101927746
Gene Name
uncharacterized LOC101927746
There are no transcripts associated with this gene.

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