Product Details

SNP ID

rs199618668

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.19:21809199 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CATTTGTAGAATTTCTCTCCAGTGC[A/G]AATTATCTTATGGGTAGTAAGGATT

Phenotype

MIM: 603972

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

ZNF43 PubMed Links

Gene Details

Gene

ZNF43

Gene Name

zinc finger protein 43

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001256648.1	6666	Intron			NP_001243577.1
NM_001256649.1	6666	Missense Mutation	CGC,TGC	R274C	NP_001243578.1
NM_001256650.1	6666	Intron			NP_001243579.1
NM_001256651.1	6666	Intron			NP_001243580.1
NM_001256653.1	6666	Intron			NP_001243582.1
NM_001256654.1	6666	Missense Mutation	CGC,TGC	R215C	NP_001243583.1
NM_003423.3	6666	Missense Mutation	CGC,TGC	R280C	NP_003414.2
XM_011528257.2	6666	Intron			XP_011526559.1
XM_011528259.2	6666	Missense Mutation	CGC,TGC	R274C	XP_011526561.1
XM_017027207.1	6666	Intron			XP_016882696.1
XM_017027208.1	6666	Intron			XP_016882697.1
XM_017027209.1	6666	Intron			XP_016882698.1
XM_017027210.1	6666	Intron			XP_016882699.1
XM_017027211.1	6666	Missense Mutation	CGC,TGC	R274C	XP_016882700.1
XM_017027212.1	6666	Intron			XP_016882701.1
XM_017027213.1	6666	Intron			XP_016882702.1
XM_017027214.1	6666	Intron			XP_016882703.1
XM_017027215.1	6666	Intron			XP_016882704.1
XM_017027216.1	6666	Intron			XP_016882705.1

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