Product Details

SNP ID

rs144634558

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.5:896683 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

ATTTTAGCCCATCGATTTGAGTGCA[C/T]GCACTGTTGCACTTCACATTTTCCA

Phenotype

MIM: 604507

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

BRD9 PubMed Links

Gene Details

Gene

BRD9

Gene Name

bromodomain containing 9

There are no transcripts associated with this gene.

Gene

TRIP13

Gene Name

thyroid hormone receptor interactor 13

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001166260.1	422	Missense Mutation	CGC,TGC	R93C	NP_001159732.1
NM_004237.3	422	Missense Mutation	CGC,TGC	R93C	NP_004228.1
XM_011514163.2	422	Missense Mutation	CGC,TGC	R93C	XP_011512465.1

View Full Product Details