Product Details

SNP ID
rs201876347
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.8:144522504 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CAGTGGATCTCGTAGGCGACCGGCG[G/T]GGGCACGCGGAGTCCCGGCCCCGCC
Phenotype
MIM: 615880 MIM: 603780
Polymorphism
G/T, Transversion Substitution
Allele Nomenclature
Literature Links
ARHGAP39 PubMed Links
Additional Information
For this assay, SNP(s) [rs13277542] 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
ARHGAP39
Gene Name
Rho GTPase activating protein 39
There are no transcripts associated with this gene.

Gene
C8orf82
Gene Name
chromosome 8 open reading frame 82
There are no transcripts associated with this gene.

Gene
LRRC14
Gene Name
leucine rich repeat containing 14
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001272036.1 1645 UTR 3 NP_001258965.1
NM_014665.3 1645 UTR 3 NP_055480.1
XM_005272358.4 1645 UTR 3 XP_005272415.1
XM_005272359.4 1645 UTR 3 XP_005272416.1
XM_005272360.4 1645 UTR 3 XP_005272417.1
XM_017014005.1 1645 UTR 3 XP_016869494.1
Gene
LRRC24
Gene Name
leucine rich repeat containing 24
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001024678.3 1645 Missense Mutation ACG,CCG T505P NP_001019849.2
Gene
RECQL4
Gene Name
RecQ like helicase 4
There are no transcripts associated with this gene.

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