Product Details

SNP ID

rs13066173

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.3:42554347 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

ATTTCTTTTTGCATAATCAGGTAAT[G/T]CTTTTTCATTTTTTTTAGGCAATGT

Phenotype

MIM: 604028

Polymorphism

G/T, Transversion Substitution

Allele Nomenclature

Literature Links

SEC22C PubMed Links

Additional Information

For this assay, SNP(s) [rs114494769] 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

SEC22C

Gene Name

SEC22 homolog C, vesicle trafficking protein

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001201572.1		Intron			NP_001188501.1
NM_001201584.1		Intron			NP_001188513.1
NM_004206.3		Intron			NP_004197.1
NM_032970.3		Intron			NP_116752.1
XM_005265533.1		Intron			XP_005265590.1
XM_005265534.1		Intron			XP_005265591.1
XM_005265535.1		Intron			XP_005265592.1
XM_011534212.1		Intron			XP_011532514.1
XM_017007438.1		Intron			XP_016862927.1
XM_017007439.1		Intron			XP_016862928.1

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