Product Details

SNP ID

rs117999319

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.7:11371743 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GCATGGACATTTTTACAGAAAAGGG[C/G]TTTTTTTTTTTTTTTTTTCCTGCAT

Phenotype

MIM: 612249

Polymorphism

C/G, Transversion Substitution

Allele Nomenclature

Literature Links

THSD7A PubMed Links

Additional Information

For this assay, SNP(s) [rs530610921] 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

THSD7A

Gene Name

thrombospondin type 1 domain containing 7A

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_015204.2	9042	UTR 3			NP_056019.1
XM_006715659.1	9042	UTR 3			XP_006715722.1
XM_006715660.1	9042	UTR 3			XP_006715723.1
XM_006715662.1	9042	UTR 3			XP_006715725.1
XM_011515193.2	9042	UTR 3			XP_011513495.1
XM_011515194.1	9042	UTR 3			XP_011513496.1

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