Product Details

SNP ID
rs1062671
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.10:20783203 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TTTTTTTAAATGATGCTTTTAAAAA[C/T]AGCACTTTGGTTTTATACATATAAT
Phenotype
MIM: 605491
Polymorphism
C/T, Transition Substitution
Allele Nomenclature
Literature Links
NEBL PubMed Links
Additional Information
For this assay, SNP(s) [rs140861015] 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
NEBL
Gene Name
nebulette
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001173484.1 5982 UTR 3 NP_001166955.1
NM_006393.2 5982 UTR 3 NP_006384.1
NM_213569.2 5982 UTR 3 NP_998734.1
XM_005252342.4 5982 UTR 3 XP_005252399.1
XM_005252343.4 5982 UTR 3 XP_005252400.1
XM_005252344.4 5982 UTR 3 XP_005252401.1
XM_011519291.2 5982 UTR 3 XP_011517593.1
XM_017015467.1 5982 UTR 3 XP_016870956.1
XM_017015468.1 5982 UTR 3 XP_016870957.1
XM_017015469.1 5982 Intron XP_016870958.1

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