Product Details

SNP ID

rs139060598

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.10:30845065 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TCCTCACAGTTATGCTGGTGCTTCC[A/G]GTGGTGGAGGAGGTCCTCTTTCCGT

Phenotype

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

ZNF438 PubMed Links

Gene Details

Gene

ZNF438

Gene Name

zinc finger protein 438

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001143766.1	2858	Missense Mutation	CGG,TGG	R795W	NP_001137238.1
NM_001143767.1	2858	Missense Mutation	CGG,TGG	R795W	NP_001137239.1
NM_001143768.1	2858	Missense Mutation	CGG,TGG	R795W	NP_001137240.1
NM_001143769.1	2858	Missense Mutation	CGG,TGG	R746W	NP_001137241.1
NM_001143770.1	2858	Missense Mutation	CGG,TGG	R785W	NP_001137242.1
NM_001143771.1	2858	Missense Mutation	CGG,TGG	R785W	NP_001137243.1
NM_182755.2	2858	Missense Mutation	CGG,TGG	R795W	NP_877432.1
XM_006717393.3	2858	Missense Mutation	CGG,TGG	R795W	XP_006717456.1
XM_006717396.3	2858	Missense Mutation	CGG,TGG	R795W	XP_006717459.1
XM_006717398.3	2858	Missense Mutation	CGG,TGG	R785W	XP_006717461.1
XM_006717399.3	2858	Missense Mutation	CGG,TGG	R785W	XP_006717462.1
XM_011519371.2	2858	Missense Mutation	CGG,TGG	R795W	XP_011517673.1
XM_011519372.2	2858	Missense Mutation	CGG,TGG	R795W	XP_011517674.1
XM_011519373.2	2858	Missense Mutation	CGG,TGG	R795W	XP_011517675.1
XM_011519374.2	2858	Missense Mutation	CGG,TGG	R795W	XP_011517676.1
XM_011519376.2	2858	Missense Mutation	CGG,TGG	R785W	XP_011517678.1
XM_011519377.2	2858	Missense Mutation	CGG,TGG	R785W	XP_011517679.1
XM_017015863.1	2858	Missense Mutation	CGG,TGG	R806W	XP_016871352.1
XM_017015864.1	2858	Missense Mutation	CGG,TGG	R795W	XP_016871353.1
XM_017015865.1	2858	Missense Mutation	CGG,TGG	R795W	XP_016871354.1
XM_017015866.1	2858	Missense Mutation	CGG,TGG	R795W	XP_016871355.1
XM_017015867.1	2858	Missense Mutation	CGG,TGG	R795W	XP_016871356.1
XM_017015868.1	2858	Missense Mutation	CGG,TGG	R795W	XP_016871357.1
XM_017015869.1	2858	Missense Mutation	CGG,TGG	R795W	XP_016871358.1
XM_017015870.1	2858	Missense Mutation	CGG,TGG	R795W	XP_016871359.1
XM_017015871.1	2858	Missense Mutation	CGG,TGG	R795W	XP_016871360.1
XM_017015872.1	2858	Missense Mutation	CGG,TGG	R795W	XP_016871361.1
XM_017015873.1	2858	Missense Mutation	CGG,TGG	R785W	XP_016871362.1
XM_017015874.1	2858	Missense Mutation	CGG,TGG	R785W	XP_016871363.1
XM_017015875.1	2858	Missense Mutation	CGG,TGG	R359W	XP_016871364.1
XM_017015876.1	2858	Missense Mutation	CGG,TGG	R359W	XP_016871365.1
XM_017015877.1	2858	Missense Mutation	CGG,TGG	R359W	XP_016871366.1
XM_017015878.1	2858	Missense Mutation	CGG,TGG	R359W	XP_016871367.1
XM_017015879.1	2858	Missense Mutation	CGG,TGG	R359W	XP_016871368.1
XM_017015880.1	2858	Missense Mutation	CGG,TGG	R359W	XP_016871369.1
XM_017015881.1	2858	Missense Mutation	CGG,TGG	R359W	XP_016871370.1
XM_017015882.1	2858	Missense Mutation	CGG,TGG	R359W	XP_016871371.1

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