Product Details

SNP ID
rs145363262
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.2:96877995 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TGGCCTGGGGGCTCTCCCGGATCTG[C/T]GTGCTGATGTGGCGGTCCAACTGCA
Phenotype
MIM: 604462
Polymorphism
C/T, Transition Substitution
Allele Nomenclature
Literature Links
FAM178B PubMed Links
Additional Information
For this assay, SNP(s) [rs574726843] are located under a primer sequence. To help evaluate the possible impact of a given SNP on your experiment, please refer to the 1000 Genomes and NCBI dbSNP databases. A higher minor allele frequency in your study population represents a higher risk to assay performance.

Gene Details

Gene
FAM178B
Gene Name
family with sequence similarity 178 member B
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001122646.2 354 Silent Mutation NP_001116118.2
NM_001172667.1 354 Silent Mutation NP_001166138.1
NM_016490.4 354 Silent Mutation NP_057574.2
XM_011511294.2 354 Silent Mutation XP_011509596.1
XM_011511297.2 354 Intron XP_011509599.1
XM_017004263.1 354 Silent Mutation XP_016859752.1
XM_017004264.1 354 Silent Mutation XP_016859753.1
XM_017004265.1 354 Intron XP_016859754.1
XM_017004266.1 354 Silent Mutation XP_016859755.1
XM_017004267.1 354 Silent Mutation XP_016859756.1
XM_017004268.1 354 Silent Mutation XP_016859757.1
Gene
SEMA4C
Gene Name
semaphorin 4C
There are no transcripts associated with this gene.

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