Product Details

SNP ID

rs298987

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.4:118727489 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

ATCTCCATGCTTAGTCTTGCCTCTT[C/T]TCTGCAAATGCCCAGTTGGAGGGAT

Phenotype

MIM: 607186

Polymorphism

C/T, Transition Substitution

Allele Nomenclature

Literature Links

SEC24D PubMed Links

Additional Information

For this assay, SNP(s) [rs78764721] 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

SEC24D

Gene Name

SEC24 homolog D, COPII coat complex component

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001318066.1		Intron			NP_001304995.1
NM_014822.3		Intron			NP_055637.2
XM_005263379.2		Intron			XP_005263436.1
XM_017008875.1		Intron			XP_016864364.1

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