Product Details

SNP ID
rs11635308
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.15:49426531 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
TTAGGATCAACAATATCTTCAACTG[G/T]AATACATTTGCATATGTAAATTTTA
Phenotype
MIM: 148180
Polymorphism
G/T, Transversion Substitution
Allele Nomenclature
Literature Links
FAM227B PubMed Links
Additional Information
For this assay, SNP(s) [rs78458957] 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
FAM227B
Gene Name
family with sequence similarity 227 member B
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_152647.2 Intron NP_689860.2
XM_005254213.3 Intron XP_005254270.1
XM_005254214.3 Intron XP_005254271.1
XM_005254215.3 Intron XP_005254272.1
XM_005254216.3 Intron XP_005254273.1
XM_005254219.3 Intron XP_005254276.1
XM_005254220.3 Intron XP_005254277.1
XM_006720423.2 Intron XP_006720486.1
XM_006720424.2 Intron XP_006720487.1
XM_006720426.2 Intron XP_006720489.1
XM_006720427.3 Intron XP_006720490.1
XM_011521319.2 Intron XP_011519621.1
XM_011521320.1 Intron XP_011519622.1
XM_011521321.2 Intron XP_011519623.1
XM_011521322.1 Intron XP_011519624.1
XM_011521324.1 Intron XP_011519626.1
XM_011521325.2 Intron XP_011519627.1
XM_011521326.1 Intron XP_011519628.1
XM_017021990.1 Intron XP_016877479.1
XM_017021991.1 Intron XP_016877480.1
XM_017021992.1 Intron XP_016877481.1
XM_017021993.1 Intron XP_016877482.1
XM_017021994.1 Intron XP_016877483.1
XM_017021995.1 Intron XP_016877484.1
XM_017021996.1 Intron XP_016877485.1
Gene
FGF7
Gene Name
fibroblast growth factor 7
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_002009.3 Intron NP_002000.1

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