Product Details

SNP ID: rs2760901
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.13:27426370 on Build GRCh38
Set Membership: HapMap
Context Sequence [VIC/FAM]: TGTAGCTCACTGTGTTCCTGTTTGC[G/T]TGTTTTGCTCCTAGTACTCTCATGG
Phenotype: MIM: 600860
Polymorphism: G/T, Transversion substitution
Allele Nomenclature
Literature Links: GTF3A PubMed Links

Gene Details

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_002097.2		Intron			NP_002088.2

There are no transcripts associated with this gene.