Product Details

SNP ID

rs200178385

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.19:9413744 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GTGAGTTCTTGTATGTTCACTAAGG[C/T]GAGAGGATCTGGCAAAGGCCTTTCC

Phenotype

MIM: 604751

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

ZNF266 PubMed Links

Gene Details

Gene

ZNF266

Gene Name

zinc finger protein 266

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001271314.1	2040	Missense Mutation	CAC,CGC	H394R	NP_001258243.1
NM_006631.3	2040	Missense Mutation	CAC,CGC	H394R	NP_006622.2
XM_005259716.3	2040	Missense Mutation	CAC,CGC	H394R	XP_005259773.1
XM_006722620.2	2040	Missense Mutation	CAC,CGC	H461R	XP_006722683.1
XM_006722621.2	2040	Missense Mutation	CAC,CGC	H461R	XP_006722684.1
XM_006722622.2	2040	Missense Mutation	CAC,CGC	H461R	XP_006722685.1
XM_006722623.3	2040	Missense Mutation	CAC,CGC	H461R	XP_006722686.1
XM_006722627.2	2040	Missense Mutation	CAC,CGC	H394R	XP_006722690.1
XM_006722630.2	2040	Missense Mutation	CAC,CGC	H394R	XP_006722693.1
XM_011527644.1	2040	Missense Mutation	CAC,CGC	H461R	XP_011525946.1
XM_011527647.1	2040	Missense Mutation	CAC,CGC	H394R	XP_011525949.1
XM_011527648.1	2040	Missense Mutation	CAC,CGC	H394R	XP_011525950.1
XM_011527650.1	2040	Missense Mutation	CAC,CGC	H394R	XP_011525952.1
XM_017026154.1	2040	Missense Mutation	CAC,CGC	H461R	XP_016881643.1
XM_017026155.1	2040	Missense Mutation	CAC,CGC	H461R	XP_016881644.1
XM_017026156.1	2040	Missense Mutation	CAC,CGC	H394R	XP_016881645.1
XM_017026157.1	2040	Missense Mutation	CAC,CGC	H394R	XP_016881646.1
XM_017026158.1	2040	Missense Mutation	CAC,CGC	H394R	XP_016881647.1
XM_017026159.1	2040	Missense Mutation	CAC,CGC	H394R	XP_016881648.1
XM_017026160.1	2040	Missense Mutation	CAC,CGC	H394R	XP_016881649.1
XM_017026161.1	2040	Missense Mutation	CAC,CGC	H394R	XP_016881650.1
XM_017026162.1	2040	Missense Mutation	CAC,CGC	H394R	XP_016881651.1
XM_017026163.1	2040	Missense Mutation	CAC,CGC	H394R	XP_016881652.1
XM_017026164.1	2040	Missense Mutation	CAC,CGC	H394R	XP_016881653.1
XM_017026165.1	2040	Missense Mutation	CAC,CGC	H394R	XP_016881654.1
XM_017026166.1	2040	Missense Mutation	CAC,CGC	H394R	XP_016881655.1
XM_017026167.1	2040	Missense Mutation	CAC,CGC	H394R	XP_016881656.1
XM_017026168.1	2040	Missense Mutation	CAC,CGC	H164R	XP_016881657.1
XM_017026169.1	2040	Missense Mutation	CAC,CGC	H164R	XP_016881658.1
XM_017026170.1	2040	Missense Mutation	CAC,CGC	H164R	XP_016881659.1
XM_017026171.1	2040	Missense Mutation	CAC,CGC	H164R	XP_016881660.1
XM_017026172.1	2040	Missense Mutation	CAC,CGC	H164R	XP_016881661.1
XM_017026173.1	2040	UTR 3			XP_016881662.1

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