Product Details

SNP ID

rs150177570

Assay Type

Functionally tested

NCBI dbSNP Submissions

2

Location

Chr.1:160999406 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CAGCACCTCACTCACCCTTTCTTTG[C/T]TCCTGAAAGAGAAGAAATGGGATCA

Phenotype

MIM: 605721

Polymorphism

C/T, 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	1075	Missense Mutation	ACA,GCA	T269A	NP_058642.1

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