Product Details

SNP ID
rs2122031
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.3:11272457 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TAAGTGAGCCGCGGCGGGCGAGGGT[A/G]TAGTGGGGTCTTGCTGGGCCGGTTT
Phenotype
MIM: 608760 MIM: 600167
Polymorphism
A/G, Transition Substitution
Allele Nomenclature
Literature Links
ATG7 PubMed Links
Additional Information
For this assay, SNP(s) [rs111373406] are located under a probe 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
ATG7
Gene Name
autophagy related 7
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001136031.2 35 Intron NP_001129503.2
NM_001144912.1 35 Intron NP_001138384.1
NM_006395.2 35 Intron NP_006386.1
XM_006712931.3 35 Intron XP_006712994.1
XM_006712932.3 35 Intron XP_006712995.1
XM_006712933.3 35 UTR 5 XP_006712996.1
XM_011533277.2 35 Intron XP_011531579.1
XM_011533278.2 35 Intron XP_011531580.1
XM_011533279.2 35 Intron XP_011531581.1
XM_011533280.2 35 Intron XP_011531582.1
XM_011533281.2 35 Intron XP_011531583.1
XM_011533282.2 35 Intron XP_011531584.1
XM_011533283.2 35 Intron XP_011531585.1
XM_011533284.2 35 Intron XP_011531586.1
XM_011533285.2 35 Intron XP_011531587.1
XM_011533286.2 35 Intron XP_011531588.1
XM_017005542.1 35 Intron XP_016861031.1
XM_017005543.1 35 Intron XP_016861032.1
XM_017005544.1 35 Intron XP_016861033.1
XM_017005545.1 35 Intron XP_016861034.1
XM_017005546.1 35 Intron XP_016861035.1
XM_017005547.1 35 Intron XP_016861036.1
XM_017005548.1 35 Intron XP_016861037.1
XM_017005549.1 35 Intron XP_016861038.1
XM_017005550.1 35 Intron XP_016861039.1
XM_017005551.1 35 Intron XP_016861040.1
XM_017005552.1 35 Intron XP_016861041.1
XM_017005553.1 35 Intron XP_016861042.1
XM_017005554.1 35 Intron XP_016861043.1
Gene
HRH1
Gene Name
histamine receptor H1
There are no transcripts associated with this gene.

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