Product Details

SNP ID

rs149886220

Assay Type

Functionally tested

NCBI dbSNP Submissions

13

Location

Chr.1:203342399 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CAGAGGGGCGCGTCGGCAGGCATGG[C/T]GCTGCGCTTGATCTCGTTCCCGTCC

Phenotype

MIM: 600245

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

FMOD PubMed Links

Gene Details

Gene

FMOD

Gene Name

fibromodulin

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_002023.4	1479	Missense Mutation			NP_002014.2

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