Product Details

SNP ID
rs112653404
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.7:87195556 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
ATGAGTCTTTTCAACATGGTCTTCA[A/G]CATGGTCTAGAGCTTACCAGTGATC
Phenotype
MIM: 608491 MIM: 616993
Polymorphism
A/G, Transition Substitution
Allele Nomenclature
Literature Links
DMTF1 PubMed Links
Additional Information
For this assay, SNP(s) [rs148183534] 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
DMTF1
Gene Name
cyclin D binding myb like transcription factor 1
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001142326.1 4213 UTR 3 NP_001135798.1
NM_001142327.1 4213 UTR 3 NP_001135799.1
NM_021145.3 4213 UTR 3 NP_066968.3
XM_011516735.2 4213 UTR 3 XP_011515037.1
XM_011516737.1 4213 UTR 3 XP_011515039.1
XM_011516739.2 4213 UTR 3 XP_011515041.1
XM_017012865.1 4213 UTR 3 XP_016868354.1
XM_017012866.1 4213 UTR 3 XP_016868355.1
XM_017012867.1 4213 UTR 3 XP_016868356.1
XM_017012868.1 4213 UTR 3 XP_016868357.1
XM_017012869.1 4213 UTR 3 XP_016868358.1
XM_017012870.1 4213 UTR 3 XP_016868359.1
XM_017012871.1 4213 UTR 3 XP_016868360.1
XM_017012872.1 4213 UTR 3 XP_016868361.1
XM_017012873.1 4213 UTR 3 XP_016868362.1
XM_017012874.1 4213 UTR 3 XP_016868363.1
XM_017012875.1 4213 UTR 3 XP_016868364.1
XM_017012876.1 4213 UTR 3 XP_016868365.1
XM_017012877.1 4213 UTR 3 XP_016868366.1
XM_017012878.1 4213 UTR 3 XP_016868367.1
Gene
TMEM243
Gene Name
transmembrane protein 243
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
XM_005250586.3 4213 Intron XP_005250643.1
XM_005250587.4 4213 Intron XP_005250644.1
XM_005250588.3 4213 Intron XP_005250645.1
XM_005250589.3 4213 Intron XP_005250646.1
XM_017012616.1 4213 Intron XP_016868105.1
XM_017012617.1 4213 Intron XP_016868106.1
XM_017012618.1 4213 Intron XP_016868107.1

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