Product Details

SNP ID
rs3820594
Assay Type
Validated
NCBI dbSNP Submissions
61
Location
Chr.1:155859720 on Build GRCh38
Set Membership
HapMap JSNP Validated
Context Sequence [VIC/FAM]
TGACCGAGGGTTCCCAGAGCTGTCT[C/T]ACCATTGCAAAAACGTTATAGCAAC
Phenotype
MIM: 610393 MIM: 608741
Polymorphism
C/T, Transition Substitution
Allele Nomenclature
Literature Links
GON4L PubMed Links
Additional Information
For this assay, SNP(s) [rs16837068] 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
GON4L
Gene Name
gon-4 like
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001282856.1 267 Intron NP_001269785.1
NM_001282858.1 267 Intron NP_001269787.1
NM_001282860.1 267 Intron NP_001269789.1
NM_001282861.1 267 Intron NP_001269790.1
NM_032292.5 267 Intron NP_115668.4
XM_005245284.3 267 Intron XP_005245341.1
XM_005245286.3 267 Intron XP_005245343.1
XM_006711393.3 267 Intron XP_006711456.1
XM_006711394.3 267 Intron XP_006711457.1
XM_011509658.2 267 Intron XP_011507960.1
XM_011509659.2 267 Intron XP_011507961.1
Gene
SYT11
Gene Name
synaptotagmin 11
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_152280.4 267 UTR 5 NP_689493.3
XM_005245014.2 267 UTR 5 XP_005245071.1
XM_017000759.1 267 UTR 5 XP_016856248.1

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