Product Details

SNP ID
rs75321673
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.4:112637718 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CTAACACTTGCTAGATATGGTGTGC[A/G]GAGTGCGTTTGCAAAGAAACTTAAG
Phenotype
MIM: 612026
Polymorphism
A/G, Transition Substitution
Allele Nomenclature
Literature Links
LARP7 PubMed Links
Additional Information
For this assay, SNP(s) [rs145318620] 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
LARP7
Gene Name
La ribonucleoprotein domain family member 7
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001267039.1 351 UTR 5 NP_001253968.1
NM_015454.2 351 Intron NP_056269.1
NM_016648.3 351 Intron NP_057732.2
Gene
ZGRF1
Gene Name
zinc finger GRF-type containing 1
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_018392.4 351 Intron NP_060862.3
XM_005263115.3 351 Intron XP_005263172.1
XM_011532091.2 351 Intron XP_011530393.1
XM_011532092.2 351 Intron XP_011530394.1
XM_011532093.2 351 Intron XP_011530395.1
XM_011532094.2 351 Intron XP_011530396.1
XM_011532096.2 351 Intron XP_011530398.1
XM_011532097.2 351 Intron XP_011530399.1
XM_011532098.2 351 Intron XP_011530400.1
XM_011532099.2 351 Intron XP_011530401.1
XM_017008369.1 351 Intron XP_016863858.1
XM_017008370.1 351 Intron XP_016863859.1
XM_017008371.1 351 Intron XP_016863860.1
XM_017008372.1 351 Intron XP_016863861.1
XM_017008373.1 351 Intron XP_016863862.1

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