Product Details

SNP ID

rs183942717

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.7:91941119 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GAGGCCATGGAGGACGAGGAGAGAC[A/G]GAAGAAGCTGGAGGCCGGCAAAGCC

Phenotype

MIM: 604001

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

AKAP9 PubMed Links

Gene Details

Gene

AKAP9

Gene Name

A-kinase anchoring protein 9

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_005751.4	253	Missense Mutation	CAG,CGG	Q7R	NP_005742.4
NM_147185.2	253	Missense Mutation	CAG,CGG	Q7R	NP_671714.1
XM_017011642.1	253	Missense Mutation	CAG,CGG	Q7R	XP_016867131.1
XM_017011643.1	253	Missense Mutation	CAG,CGG	Q7R	XP_016867132.1
XM_017011644.1	253	Missense Mutation	CAG,CGG	Q7R	XP_016867133.1
XM_017011645.1	253	Missense Mutation	CAG,CGG	Q7R	XP_016867134.1
XM_017011646.1	253	Missense Mutation	CAG,CGG	Q7R	XP_016867135.1
XM_017011647.1	253	Missense Mutation	CAG,CGG	Q7R	XP_016867136.1
XM_017011648.1	253	Missense Mutation	CAG,CGG	Q7R	XP_016867137.1
XM_017011649.1	253	Missense Mutation	CAG,CGG	Q7R	XP_016867138.1
XM_017011650.1	253	Missense Mutation	CAG,CGG	Q7R	XP_016867139.1
XM_017011651.1	253	Missense Mutation	CAG,CGG	Q7R	XP_016867140.1
XM_017011652.1	253	Missense Mutation	CAG,CGG	Q7R	XP_016867141.1
XM_017011653.1	253	Missense Mutation	CAG,CGG	Q7R	XP_016867142.1
XM_017011654.1	253	Missense Mutation	CAG,CGG	Q7R	XP_016867143.1
XM_017011655.1	253	Intron			XP_016867144.1
XM_017011656.1	253	Intron			XP_016867145.1
XM_017011657.1	253	Intron			XP_016867146.1
XM_017011658.1	253	Intron			XP_016867147.1
XM_017011659.1	253	Intron			XP_016867148.1
XM_017011660.1	253	Intron			XP_016867149.1

View Full Product Details