Product Details

SNP ID

rs17032644

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.3:10304379 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

AGTCTCCCGGATTCCTTTTCTCATC[C/T]GGGTTTCGGAGGTGGACTCTGTCTG

Phenotype

MIM: 600152

Polymorphism

C/T, Transition Substitution

Allele Nomenclature

Literature Links

SEC13 PubMed Links

Additional Information

For this assay, SNP(s) [rs112628776] are located under a probe 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

SEC13

Gene Name

SEC13 homolog, nuclear pore and COPII coat complex component

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001136026.2		Intron			NP_001129498.1
NM_001136232.2		Intron			NP_001129704.1
NM_001278946.1		Intron			NP_001265875.1
NM_030673.3		Intron			NP_109598.2
NM_183352.2		Intron			NP_899195.1
XM_005265379.2		Intron			XP_005265436.1
XM_017007019.1		Intron			XP_016862508.1
XM_017007020.1		Intron			XP_016862509.1
XM_017007021.1		Intron			XP_016862510.1

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