Product Details

SNP ID

rs2683324

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.8:19314706 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

TTAATAGAAACAACGACTTGGGTAC[C/G]ATTATTTTAAAATAGTGAATAAATA

Phenotype

MIM: 614968

Polymorphism

C/G, Transversion Substitution

Allele Nomenclature

Literature Links

SH2D4A PubMed Links

Additional Information

For this assay, SNP(s) [rs75229377] 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

SH2D4A

Gene Name

SH2 domain containing 4A

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001174159.1		Intron			NP_001167630.1
NM_001174160.1		Intron			NP_001167631.1
NM_022071.3		Intron			NP_071354.2
XM_011544610.1		Intron			XP_011542912.1
XM_017013729.1		Intron			XP_016869218.1

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