Product Details

SNP ID

rs113687833

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.22:37051815 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GCCGGCGGGGGCGGGCGGCCGCGCC[A/G]CAGGCGGCTGGGGCAAGTGGGTGCG

Phenotype

MIM: 616386

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

KCTD17 PubMed Links

Gene Details

Gene

KCTD17

Gene Name

potassium channel tetramerization domain containing 17

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001282684.1	91	Missense Mutation	ACA,GCA	T26A	NP_001269613.1
NM_001282685.1	91	Missense Mutation	ACA,GCA	T26A	NP_001269614.1
NM_001282686.1	91	Missense Mutation	ACA,GCA	T26A	NP_001269615.1
NM_024681.3	91	Missense Mutation	ACA,GCA	T26A	NP_078957.2
XM_005261741.3	91	Missense Mutation	ACA,GCA	T26A	XP_005261798.2
XM_005261742.2	91	Missense Mutation	ACA,GCA	T26A	XP_005261799.2
XM_005261743.2	91	Missense Mutation	ACA,GCA	T26A	XP_005261800.2
XM_005261744.2	91	Missense Mutation	ACA,GCA	T26A	XP_005261801.1
XM_011530374.2	91	Missense Mutation	ACA,GCA	T26A	XP_011528676.1
XM_011530377.2	91	Missense Mutation	ACA,GCA	T26A	XP_011528679.1

View Full Product Details