Product Details

SNP ID

rs17852877

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.22:37051890 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CCTGACCACCCGGCAGACGCTGTGC[C/G]GCGAGCAGAAGTCCTTCCTCAGCCG

Phenotype

MIM: 616386

Polymorphism

C/G, Transversion 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	166	Missense Mutation	CGC,GGC	R51G	NP_001269613.1
NM_001282685.1	166	Missense Mutation	CGC,GGC	R51G	NP_001269614.1
NM_001282686.1	166	Missense Mutation	CGC,GGC	R51G	NP_001269615.1
NM_024681.3	166	Missense Mutation	CGC,GGC	R51G	NP_078957.2
XM_005261741.3	166	Missense Mutation	CGC,GGC	R51G	XP_005261798.2
XM_005261742.2	166	Missense Mutation	CGC,GGC	R51G	XP_005261799.2
XM_005261743.2	166	Missense Mutation	CGC,GGC	R51G	XP_005261800.2
XM_005261744.2	166	Missense Mutation	CGC,GGC	R51G	XP_005261801.1
XM_011530374.2	166	Missense Mutation	CGC,GGC	R51G	XP_011528676.1
XM_011530377.2	166	Missense Mutation	CGC,GGC	R51G	XP_011528679.1

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