Product Details

SNP ID

rs201818632

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.16:3383085 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CCAGTGTGGATGCGCCGGTGAGCAC[C/T]GAACTGGGAACTGTTGTTGAATCTC

Phenotype

Polymorphism

C/T, 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	2124	Missense Mutation	AGT,GGT	S621G	NP_001271456.1
NM_001284528.1	2124	Missense Mutation	AGT,GGT	S332G	NP_001271457.1
NM_001284529.1	2124	Missense Mutation	AGT,GGT	S332G	NP_001271458.1
NM_001324340.1	2124	Missense Mutation	AGT,GGT	S409G	NP_001311269.1
NM_001324341.1	2124	Missense Mutation	AGT,GGT	S409G	NP_001311270.1
NM_001324342.1	2124	Missense Mutation	AGT,GGT	S409G	NP_001311271.1
NM_001324343.1	2124	Missense Mutation	AGT,GGT	S488G	NP_001311272.1
NM_001324344.1	2124	Missense Mutation	AGT,GGT	S409G	NP_001311273.1
NM_001324345.1	2124	Missense Mutation	AGT,GGT	S409G	NP_001311274.1
NM_001324346.1	2124	Missense Mutation	AGT,GGT	S548G	NP_001311275.1
NM_017810.3	2124	Missense Mutation	AGT,GGT	S409G	NP_060280.2
XM_005255403.2	2124	Missense Mutation	AGT,GGT	S534G	XP_005255460.1
XM_011522555.2	2124	Missense Mutation	AGT,GGT	S621G	XP_011520857.1
XM_017023371.1	2124	Missense Mutation	AGT,GGT	S621G	XP_016878860.1
XM_017023372.1	2124	Missense Mutation	AGT,GGT	S534G	XP_016878861.1
XM_017023373.1	2124	Missense Mutation	AGT,GGT	S534G	XP_016878862.1

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