Product Details

SNP ID
rs12338918
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.9:121212193 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
AACAAAACAGATATCCCAGCAGCTA[C/T]ACAAGCAAGCGTTTTCAGAGCTCAC
Phenotype
MIM: 137350
Polymorphism
C/T, Transition Substitution
Allele Nomenclature
Literature Links
GSN PubMed Links
Additional Information
For this assay, SNP(s) [rs114815873] 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
GSN
Gene Name
gelsolin
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_000177.4 Intron NP_000168.1
NM_001127662.1 Intron NP_001121134.1
NM_001127663.1 Intron NP_001121135.2
NM_001127664.1 Intron NP_001121136.1
NM_001127665.1 Intron NP_001121137.1
NM_001127666.1 Intron NP_001121138.1
NM_001127667.1 Intron NP_001121139.1
NM_001258029.1 Intron NP_001244958.1
NM_001258030.1 Intron NP_001244959.1
NM_198252.2 Intron NP_937895.1
XM_005251943.1 Intron XP_005252000.1
XM_005251944.1 Intron XP_005252001.1
XM_005251945.3 Intron XP_005252002.1
XM_006717079.1 Intron XP_006717142.1
XM_011518584.1 Intron XP_011516886.1
XM_011518585.1 Intron XP_011516887.1
XM_011518586.1 Intron XP_011516888.1
XM_011518587.2 Intron XP_011516889.1
XM_011518588.2 Intron XP_011516890.1
XM_011518589.2 Intron XP_011516891.1
XM_011518590.2 Intron XP_011516892.1
XM_011518591.2 Intron XP_011516893.1
XM_011518592.1 Intron XP_011516894.1
XM_011518593.1 Intron XP_011516895.1
XM_011518594.1 Intron XP_011516896.1
XM_017014643.1 Intron XP_016870132.1
XM_017014644.1 Intron XP_016870133.1
XM_017014645.1 Intron XP_016870134.1
XM_017014646.1 Intron XP_016870135.1
XM_017014647.1 Intron XP_016870136.1
XM_017014648.1 Intron XP_016870137.1

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