Product Details

SNP ID

rs118083394

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.9:120605274 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CATTGCCATCATCTTCCAACAATCC[C/T]GAAACATCTGCATTGGGAATGCTGT

Phenotype

MIM: 604268

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

MEGF9 PubMed Links

Gene Details

Gene

MEGF9

Gene Name

multiple EGF like domains 9

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001080497.2	1854	Silent Mutation	TCA,TCG	S575S	NP_001073966.2

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