Product Details

SNP ID

rs200251122

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.16:89270847 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TGCGGTCATACTTGTCATCCACGTC[C/T]TGGAGCCAGGAGATGAACTGGCGGG

Phenotype

MIM: 611192

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

ANKRD11 PubMed Links

Gene Details

Gene

ANKRD11

Gene Name

ankyrin repeat domain 11

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001256182.1	8014	Silent Mutation	CAA,CAG	Q2592Q	NP_001243111.1
NM_001256183.1	8014	Silent Mutation	CAA,CAG	Q2592Q	NP_001243112.1
NM_013275.5	8014	Silent Mutation	CAA,CAG	Q2592Q	NP_037407.4
XM_006721181.1	8014	Silent Mutation	CAA,CAG	Q2558Q	XP_006721244.1
XM_006721184.2	8014	Silent Mutation	CAA,CAG	Q2493Q	XP_006721247.1
XM_011523051.2	8014	Silent Mutation	CAA,CAG	Q2592Q	XP_011521353.1
XM_011523053.2	8014	Silent Mutation	CAA,CAG	Q2592Q	XP_011521355.1
XM_011523054.2	8014	Silent Mutation	CAA,CAG	Q2558Q	XP_011521356.1
XM_011523055.2	8014	Silent Mutation	CAA,CAG	Q2558Q	XP_011521357.1
XM_011523056.2	8014	Silent Mutation	CAA,CAG	Q2549Q	XP_011521358.1
XM_011523057.2	8014	Silent Mutation	CAA,CAG	Q2592Q	XP_011521359.1
XM_017023182.1	8014	Silent Mutation	CAA,CAG	Q2592Q	XP_016878671.1
XM_017023183.1	8014	Silent Mutation	CAA,CAG	Q2592Q	XP_016878672.1
XM_017023184.1	8014	Silent Mutation	CAA,CAG	Q2592Q	XP_016878673.1
XM_017023185.1	8014	Silent Mutation	CAA,CAG	Q2592Q	XP_016878674.1
XM_017023186.1	8014	Silent Mutation	CAA,CAG	Q2592Q	XP_016878675.1
XM_017023187.1	8014	Silent Mutation	CAA,CAG	Q2592Q	XP_016878676.1

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