Product Details

SNP ID

rs13598

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.15:48410260 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

CTCTATGCACGTGTGGGCCAGTCAC[A/C]GAAATTTCATTACCACTTGGTGTAT

Phenotype

MIM: 134797

Polymorphism

A/C, Transversion substitution

Allele Nomenclature

Literature Links

FBN1 PubMed Links

Gene Details

Gene

FBN1

Gene Name

fibrillin 1

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_000138.4	9741	UTR 3			NP_000129.3

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