Product Details

SNP ID

rs183473998

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.7:120275340 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CCTTCTTCTGCTTGGACACGGCCTG[C/T]GTCATGATCTTCACAGTTGAGTATT

Phenotype

MIM: 605410

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

KCND2 PubMed Links

Gene Details

Gene

KCND2

Gene Name

potassium voltage-gated channel subfamily D member 2

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_012281.2	1673	Silent Mutation	TGC,TGT	C236C	NP_036413.1
XM_011516165.2	1673	Silent Mutation	TGC,TGT	C236C	XP_011514467.1

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