Product Details

SNP ID

rs10902188

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.11:654043 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

TCATAGCCTCCCGGCCGCAGTTAAC[A/G]CAGGACTGCTGCAAGAAGGACACAA

Phenotype

MIM: 602635

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

DEAF1 PubMed Links

Gene Details

Gene

DEAF1

Gene Name

DEAF1, transcription factor

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001293634.1	2219	Silent Mutation	TGC,TGT	C429C	NP_001280563.1
NM_021008.3	2219	Silent Mutation	TGC,TGT	C504C	NP_066288.2
XM_011519842.2	2219	Silent Mutation	TGC,TGT	C504C	XP_011518144.1

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