Product Details

SNP ID

rs2367796

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.2:179443301 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

CAGGAGTGGCGCGGATGGGCCCATG[C/T]CCAGGCCTCAGAAGAGCTGGAGGAA

Phenotype

MIM: 612344

Polymorphism

C/T, 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	1285	Silent Mutation	GGA,GGG	G379G	NP_001106868.1
NM_001113398.1	1285	Silent Mutation	GGA,GGG	G353G	NP_001106869.1
NM_001282725.1	1285	Silent Mutation	GGA,GGG	G353G	NP_001269654.1
NM_152520.4	1285	Silent Mutation	GGA,GGG	G455G	NP_689733.3
XM_011510713.2	1285	Silent Mutation	GGA,GGG	G510G	XP_011509015.1
XM_011510714.2	1285	Silent Mutation	GGA,GGG	G497G	XP_011509016.1
XM_011510715.2	1285	Silent Mutation	GGA,GGG	G483G	XP_011509017.1
XM_011510716.2	1285	Silent Mutation	GGA,GGG	G413G	XP_011509018.1
XM_011510717.2	1285	Silent Mutation	GGA,GGG	G413G	XP_011509019.1
XM_011510719.2	1285	Silent Mutation	GGA,GGG	G393G	XP_011509021.1
XM_011510720.2	1285	Silent Mutation	GGA,GGG	G393G	XP_011509022.1
XM_011510721.2	1285	Silent Mutation	GGA,GGG	G380G	XP_011509023.1
XM_011510723.2	1285	Intron			XP_011509025.1
XM_017003435.1	1285	Silent Mutation	GGA,GGG	G470G	XP_016858924.1
XM_017003436.1	1285	Silent Mutation	GGA,GGG	G393G	XP_016858925.1
XM_017003437.1	1285	Silent Mutation	GGA,GGG	G387G	XP_016858926.1
XM_017003438.1	1285	Silent Mutation	GGA,GGG	G353G	XP_016858927.1
XM_017003439.1	1285	Silent Mutation	GGA,GGG	G353G	XP_016858928.1
XM_017003440.1	1285	Silent Mutation	GGA,GGG	G341G	XP_016858929.1
XM_017003441.1	1285	Intron			XP_016858930.1

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