Product Details

SNP ID

rs35233455

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.9:36589558 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CAGAGTGATTTGCCCCGGATCAAAA[C/T]GGAGATTGAGGCCTTGAAGAACCTG

Phenotype

MIM: 607025

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

MELK PubMed Links

Gene Details

Gene

MELK

Gene Name

maternal embryonic leucine zipper kinase

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001256685.1	351	Missense Mutation	ACG,ATG	T56M	NP_001243614.1
NM_001256687.1	351	Missense Mutation	ACG,ATG	T56M	NP_001243616.1
NM_001256688.1	351	Missense Mutation	ACG,ATG	T56M	NP_001243617.1
NM_001256689.1	351	Missense Mutation	ACG,ATG	T24M	NP_001243618.1
NM_001256690.1	351	Intron			NP_001243619.1
NM_001256691.1	351	Missense Mutation	ACG,ATG	T24M	NP_001243620.1
NM_001256692.1	351	UTR 5			NP_001243621.1
NM_001256693.1	351	UTR 5			NP_001243622.1
NM_014791.3	351	Missense Mutation	ACG,ATG	T56M	NP_055606.1
XM_011518076.2	351	Missense Mutation	ACG,ATG	T56M	XP_011516378.1
XM_011518077.1	351	Missense Mutation	ACG,ATG	T56M	XP_011516379.1
XM_011518078.2	351	Missense Mutation	ACG,ATG	T56M	XP_011516380.1
XM_011518079.1	351	Missense Mutation	ACG,ATG	T56M	XP_011516381.1
XM_011518080.1	351	Missense Mutation	ACG,ATG	T56M	XP_011516382.1
XM_011518081.2	351	Missense Mutation	ACG,ATG	T24M	XP_011516383.1
XM_011518082.2	351	Missense Mutation	ACG,ATG	T24M	XP_011516384.1
XM_011518083.2	351	Missense Mutation	ACG,ATG	T24M	XP_011516385.1
XM_011518084.2	351	Missense Mutation	ACG,ATG	T24M	XP_011516386.1
XM_011518085.1	351	UTR 5			XP_011516387.1
XM_011518086.2	351	Missense Mutation	ACG,ATG	T56M	XP_011516388.1

View Full Product Details