Product Details

SNP ID

rs201511674

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.16:3383073 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TATGGGCTCTCCCCAGTGTGGATGC[A/G]CCGGTGAGCACTGAACTGGGAACTG

Phenotype

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

ZSCAN32 PubMed Links

Gene Details

Gene

ZSCAN32

Gene Name

zinc finger and SCAN domain containing 32

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001284527.1	2136	Missense Mutation	CGC,TGC	R625C	NP_001271456.1
NM_001284528.1	2136	Missense Mutation	CGC,TGC	R336C	NP_001271457.1
NM_001284529.1	2136	Missense Mutation	CGC,TGC	R336C	NP_001271458.1
NM_001324340.1	2136	Missense Mutation	CGC,TGC	R413C	NP_001311269.1
NM_001324341.1	2136	Missense Mutation	CGC,TGC	R413C	NP_001311270.1
NM_001324342.1	2136	Missense Mutation	CGC,TGC	R413C	NP_001311271.1
NM_001324343.1	2136	Missense Mutation	CGC,TGC	R492C	NP_001311272.1
NM_001324344.1	2136	Missense Mutation	CGC,TGC	R413C	NP_001311273.1
NM_001324345.1	2136	Missense Mutation	CGC,TGC	R413C	NP_001311274.1
NM_001324346.1	2136	Missense Mutation	CGC,TGC	R552C	NP_001311275.1
NM_017810.3	2136	Missense Mutation	CGC,TGC	R413C	NP_060280.2
XM_005255403.2	2136	Missense Mutation	CGC,TGC	R538C	XP_005255460.1
XM_011522555.2	2136	Missense Mutation	CGC,TGC	R625C	XP_011520857.1
XM_017023371.1	2136	Missense Mutation	CGC,TGC	R625C	XP_016878860.1
XM_017023372.1	2136	Missense Mutation	CGC,TGC	R538C	XP_016878861.1
XM_017023373.1	2136	Missense Mutation	CGC,TGC	R538C	XP_016878862.1

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