Product Details

SNP ID

rs7987863

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.13:45120004 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

CTTACTTGTTCGTTTCGTTACAGAC[C/T]TCCGGGTTTTGGAAACTGAGGTGCT

Phenotype

MIM: 189969

Polymorphism

C/T, Transition Substitution

Allele Nomenclature

Literature Links

GTF2F2 PubMed Links

Additional Information

For this assay, SNP(s) [rs9567531] 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

GTF2F2

Gene Name

general transcription factor IIF subunit 2

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_004128.2		Intron			NP_004119.1
XM_011535052.2		Intron			XP_011533354.1
XM_011535053.2		Intron			XP_011533355.1
XM_017020550.1		Intron			XP_016876039.1
XM_017020551.1		Intron			XP_016876040.1

Gene

LOC101929259

Gene Name

uncharacterized LOC101929259

There are no transcripts associated with this gene.

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