Product Details

SNP ID

rs28450060

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.19:39454356 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GGTGGTGCATTTTGTTGTTGTCGTT[G/T]TTTTTTTTTTTTTTTTTGAGACGGA

Phenotype

MIM: 602102

Polymorphism

G/T, Transversion Substitution

Allele Nomenclature

Literature Links

SUPT5H PubMed Links

Additional Information

For this assay, SNP(s) [rs148457475] 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

SUPT5H

Gene Name

SPT5 homolog, DSIF elongation factor subunit

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001111020.2		Intron			NP_001104490.1
NM_001130824.1		Intron			NP_001124296.1
NM_001130825.1		Intron			NP_001124297.1
NM_001319990.1		Intron			NP_001306919.1
NM_001319991.1		Intron			NP_001306920.1
NM_003169.3		Intron			NP_003160.2
XM_017027174.1		Intron			XP_016882663.1

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