Product Details

SNP ID
rs734451
Assay Type
Validated
NCBI dbSNP Submissions
NA
Location
Chr.6:107701359 on Build GRCh38
Set Membership
Validated
Context Sequence [VIC/FAM]
TGGGCTCCCCGGCAATGTGTCTCCC[A/G]AGAGTCACCTGGAGCCCAGGCTTGG
Phenotype
Polymorphism
A/G, Transition Substitution
Allele Nomenclature
Literature Links
SCML4 PubMed Links
Additional Information
For this assay, SNP(s) [rs73764237] 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
SCML4
Gene Name
sex comb on midleg-like 4 (Drosophila)
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001286408.1 5079 Intron NP_001273337.1
NM_001286409.1 5079 Intron NP_001273338.1
NM_198081.4 5079 Intron NP_932347.2
XM_011535703.2 5079 UTR 3 XP_011534005.1
XM_011535704.2 5079 UTR 3 XP_011534006.1
XM_011535706.1 5079 UTR 3 XP_011534008.1
XM_011535707.2 5079 Intron XP_011534009.1
XM_011535709.2 5079 UTR 3 XP_011534011.1
XM_011535710.2 5079 UTR 3 XP_011534012.1
XM_017010677.1 5079 UTR 3 XP_016866166.1
XM_017010678.1 5079 UTR 3 XP_016866167.1
XM_017010679.1 5079 UTR 3 XP_016866168.1
XM_017010680.1 5079 UTR 3 XP_016866169.1
XM_017010681.1 5079 UTR 3 XP_016866170.1
XM_017010682.1 5079 UTR 3 XP_016866171.1
XM_017010683.1 5079 UTR 3 XP_016866172.1
XM_017010684.1 5079 Intron XP_016866173.1
XM_017010685.1 5079 UTR 3 XP_016866174.1
XM_017010686.1 5079 UTR 3 XP_016866175.1
XM_017010687.1 5079 UTR 3 XP_016866176.1
XM_017010688.1 5079 Intron XP_016866177.1

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