Product Details

SNP ID
rs201297323
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.18:63637768 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GAAGAGGATGCTGTTGGTCTTATTT[C/T]GCCTTATGAAGAATAGGAAAGGGTG
Phenotype
MIM: 600518
Polymorphism
C/T, Transition Substitution
Allele Nomenclature
Literature Links
SERPINB4 PubMed Links
Additional Information
For this assay, SNP(s) [rs58958857] 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
SERPINB4
Gene Name
serpin family B member 4
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_002974.3 1271 Missense Mutation CAA,CGA Q375R NP_002965.1
NM_175041.1 1271 Missense Mutation CAA,CGA Q354R NP_778206.1
XM_011526138.1 1271 Missense Mutation CAA,CGA Q375R XP_011524440.1

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