Product Details

SNP ID

rs17130638

Assay Type

Functionally tested

NCBI dbSNP Submissions

18

Location

Chr.1:88855880 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

CATGTTGGCCAGGAGGCTGGTCACC[A/G]CACCTAGTTTATGAATTTCTTTACA

Phenotype

MIM: 189963

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

GTF2B PubMed Links

Gene Details

Gene

GTF2B

Gene Name

general transcription factor IIB

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001514.5		Intron			NP_001505.1
XM_011541299.1		Intron			XP_011539601.1

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