Product Details

SNP ID

rs146651683

Assay Type

Functionally tested

NCBI dbSNP Submissions

3

Location

Chr.1:160998887 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CGACCAGGCTCACACCAGGAATGAC[A/G]AGGTCTGTTTGAATTCTCCCTGCAG

Phenotype

MIM: 605721

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

F11R PubMed Links

Gene Details

Gene

F11R

Gene Name

F11 receptor

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_016946.4	1154	Missense Mutation	TCG,TTG	S295L	NP_058642.1

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