Product Details

SNP ID

rs76788604

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.15:78090639 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CTTGCATCACCATCATCATCATCAT[A/C]ATCATCATCATCATCATCATCATCA

Phenotype

Polymorphism

A/C, Transversion Substitution

Allele Nomenclature

Literature Links

SH2D7 PubMed Links

Additional Information

For this assay, SNP(s) [rs149544016] 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

SH2D7

Gene Name

SH2 domain containing 7

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001101404.1		Intron			NP_001094874.1
XM_011521895.2		Intron			XP_011520197.1
XM_011521896.2		Intron			XP_011520198.1
XM_011521899.2		Intron			XP_011520201.1
XM_017022487.1		Intron			XP_016877976.1
XM_017022488.1		Intron			XP_016877977.1

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