Product Details

SNP ID

rs7798459

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.7:1048329 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

CTAACAGGGACAGCAACATCAAAAG[C/T]GATGGCTTTTGTGAAACTAATTCAG

Phenotype

Polymorphism

C/T, Transition Substitution

Allele Nomenclature

Literature Links

C7orf50 PubMed Links

Additional Information

For this assay, SNP(s) [rs79978525] 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

C7orf50

Gene Name

chromosome 7 open reading frame 50

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001134395.1		Intron			NP_001127867.1
NM_001134396.1		Intron			NP_001127868.1
NM_001318252.1		Intron			NP_001305181.1
NM_032350.5		Intron			NP_115726.1
XM_006715793.2		Intron			XP_006715856.1
XM_011515580.2		Intron			XP_011513882.1
XM_011515581.2		Intron			XP_011513883.1
XM_011515582.2		Intron			XP_011513884.1
XM_011515583.2		Intron			XP_011513885.1
XM_011515584.2		Intron			XP_011513886.1
XM_017012719.1		Intron			XP_016868208.1
XM_017012720.1		Intron			XP_016868209.1
XM_017012721.1		Intron			XP_016868210.1
XM_017012722.1		Intron			XP_016868211.1

Gene

GPR146

Gene Name

G protein-coupled receptor 146

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001303473.1		Intron			NP_001290402.1
NM_001303474.1		Intron			NP_001290403.1
NM_138445.3		Intron			NP_612454.1
XM_005249613.2		Intron			XP_005249670.1
XM_006715642.2		Intron			XP_006715705.1
XM_006715643.2		Intron			XP_006715706.1
XM_011515116.2		Intron			XP_011513418.1

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