Product Details

SNP ID

rs1497622

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.4:143577615 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

TTTTTTCCCTCTTAAAGTCTTTCAA[C/T]CAAAGGAACTACAAGCACTCTGCTT

Phenotype

MIM: 608946

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

FREM3 PubMed Links

Gene Details

Gene

FREM3

Gene Name

FRAS1 related extracellular matrix 3

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001168235.1	6416	Missense Mutation	GAT,GGT	D2139G	NP_001161707.1

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