Product Details

SNP ID

rs149044377

Assay Type

Functionally tested

NCBI dbSNP Submissions

10

Location

Chr.1:160998886 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CCGACCAGGCTCACACCAGGAATGA[C/T]GAGGTCTGTTTGAATTCTCCCTGCA

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	1155	Silent Mutation	TCA,TCG	S295S	NP_058642.1

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