Product Details

SNP ID

rs200421693

Assay Type

Functionally tested

NCBI dbSNP Submissions

1

Location

Chr.1:223110709 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

AGGTCAGATAAGCACCTGCCCTGGG[C/T]ATAACTGAAGGCTTCAAGGCACCAG

Phenotype

MIM: 603031

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

TLR5 PubMed Links

Gene Details

Gene

TLR5

Gene Name

toll like receptor 5

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_003268.5	2816	Missense Mutation	ACC,GCC	T775A	NP_003259.2
XM_005273241.4	2816	Missense Mutation	ACC,GCC	T775A	XP_005273298.2
XM_005273242.4	2816	Missense Mutation	ACC,GCC	T775A	XP_005273299.2
XM_005273243.4	2816	Missense Mutation	ACC,GCC	T775A	XP_005273300.2
XM_006711504.3	2816	Missense Mutation	ACC,GCC	T775A	XP_006711567.1
XM_006711505.3	2816	Missense Mutation	ACC,GCC	T775A	XP_006711568.1
XM_006711506.3	2816	Missense Mutation	ACC,GCC	T775A	XP_006711569.1
XM_011509937.2	2816	Missense Mutation	ACC,GCC	T775A	XP_011508239.1
XM_017002208.1	2816	Missense Mutation	ACC,GCC	T775A	XP_016857697.1

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