Product Details

SNP ID
rs137908922
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.22:36762981 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TCAGCTGAGTCCACTGCTCGTCTGC[C/T]GGCCAGGTCTGTCTTGTTCCCAACT
Phenotype
MIM: 615870
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
IFT27 PubMed Links

Gene Details

Gene
IFT27
Gene Name
intraflagellar transport 27
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001177701.2 815 Missense Mutation AGC,GGC S129G NP_001171172.1
NM_006860.4 815 Missense Mutation AGC,GGC S128G NP_006851.1
XM_006724106.2 815 Missense Mutation AGC,GGC S129G XP_006724169.1
XM_017028540.1 815 Missense Mutation AGC,GGC S88G XP_016884029.1
Gene
LOC105373021
Gene Name
uncharacterized LOC105373021
There are no transcripts associated with this gene.

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