Product Details

SNP ID

rs140852252

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.X:80676918 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TTCCCCTCCCCCTAGTGCCACCTCC[A/G]CCTCTTCCTCGACTCCCTCGTCCCC

Phenotype

MIM: 300553

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

BRWD3 PubMed Links

Gene Details

Gene

BRWD3

Gene Name

bromodomain and WD repeat domain containing 3

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_153252.4	5363	Silent Mutation	GGC,GGT	G1700G	NP_694984.4
XM_005262113.3	5363	Silent Mutation	GGC,GGT	G1650G	XP_005262170.1
XM_017029384.1	5363	Silent Mutation	GGC,GGT	G1296G	XP_016884873.1
XM_017029385.1	5363	Intron			XP_016884874.1

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