Product Details

SNP ID

rs200150920

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.2:179444896 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CTTACTGCTAGAATACTCGGGCTCC[A/G]CTGGAGTTTGTTGTAAGGGCTGTAT

Phenotype

MIM: 612344

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

ZNF385B PubMed Links

Gene Details

Gene

ZNF385B

Gene Name

zinc finger protein 385B

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001113397.1	1097	Missense Mutation	CGG,TGG	R317W	NP_001106868.1
NM_001113398.1	1097	Missense Mutation	CGG,TGG	R291W	NP_001106869.1
NM_001282725.1	1097	Missense Mutation	CGG,TGG	R291W	NP_001269654.1
NM_152520.4	1097	Missense Mutation	CGG,TGG	R393W	NP_689733.3
XM_011510713.2	1097	Missense Mutation	CGG,TGG	R448W	XP_011509015.1
XM_011510714.2	1097	Missense Mutation	CGG,TGG	R435W	XP_011509016.1
XM_011510715.2	1097	Missense Mutation	CGG,TGG	R421W	XP_011509017.1
XM_011510716.2	1097	Missense Mutation	CGG,TGG	R351W	XP_011509018.1
XM_011510717.2	1097	Missense Mutation	CGG,TGG	R351W	XP_011509019.1
XM_011510719.2	1097	Missense Mutation	CGG,TGG	R331W	XP_011509021.1
XM_011510720.2	1097	Missense Mutation	CGG,TGG	R331W	XP_011509022.1
XM_011510721.2	1097	Missense Mutation	CGG,TGG	R318W	XP_011509023.1
XM_011510723.2	1097	Intron			XP_011509025.1
XM_017003435.1	1097	Missense Mutation	CGG,TGG	R408W	XP_016858924.1
XM_017003436.1	1097	Missense Mutation	CGG,TGG	R331W	XP_016858925.1
XM_017003437.1	1097	Missense Mutation	CGG,TGG	R325W	XP_016858926.1
XM_017003438.1	1097	Missense Mutation	CGG,TGG	R291W	XP_016858927.1
XM_017003439.1	1097	Missense Mutation	CGG,TGG	R291W	XP_016858928.1
XM_017003440.1	1097	Missense Mutation	CGG,TGG	R279W	XP_016858929.1
XM_017003441.1	1097	Intron			XP_016858930.1

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