Product Details

SNP ID

rs9929532

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.16:28573241 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

GGACCTGGGGGGGTGTAAGAGATAG[C/G]CAGGCTCCAGCCCAGAGGAGGAGCT

Phenotype

MIM: 613374

Polymorphism

C/G, Transversion substitution

Allele Nomenclature

Literature Links

SGF29 PubMed Links

Gene Details

Gene

SGF29

Gene Name

SAGA complex associated factor 29

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_138414.2		Intron			NP_612423.1
XM_017022894.1		Intron			XP_016878383.1

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