Product Details

SNP ID

rs186347987

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.17:42207574 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CATTGTTACCAGTAGCAGACTCGCA[A/G]GGAACTGGTGTGTAGTATTTGGAGT

Phenotype

MIM: 604260

Polymorphism

A/G, Transition Substitution

Allele Nomenclature

Literature Links

STAT5B PubMed Links

Additional Information

For this assay, SNP(s) [rs536097228] 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

STAT5B

Gene Name

signal transducer and activator of transcription 5B

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_012448.3	2049	Silent Mutation	CCC,CCT	P687P	NP_036580.2
XM_005257626.4	2049	Intron			XP_005257683.1
XM_017024977.1	2049	Silent Mutation	CCC,CCT	P593P	XP_016880466.1

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