Product Details

SNP ID

rs200406151

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.11:3360267 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GCATTTGAAAGGATTTGCCACATTC[G/T]TGACATTTGAAAGGTTTCTCTCCAG

Phenotype

MIM: 602187

Polymorphism

G/T, Transversion substitution

Allele Nomenclature

Literature Links

ZNF195 PubMed Links

Gene Details

Gene

ZNF195

Gene Name

zinc finger protein 195

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001130519.2	1260	Missense Mutation	CAA,CAC	Q224H	NP_001123991.1
NM_001130520.2	1260	Missense Mutation	CAA,CAC	Q247H	NP_001123992.1
NM_001242841.1	1260	Missense Mutation	CAA,CAC	Q228H	NP_001229770.1
NM_001242842.1	1260	Missense Mutation	CAA,CAC	Q202H	NP_001229771.1
NM_001242843.1	1260	Missense Mutation	CAA,CAC	Q179H	NP_001229772.1
NM_001256823.1	1260	UTR 3			NP_001243752.1
NM_001256824.1	1260	Missense Mutation	CAA,CAC	Q210H	NP_001243753.1
NM_001256825.1	1260	Missense Mutation	CAA,CAC	Q179H	NP_001243754.1
NM_007152.4	1260	Missense Mutation	CAA,CAC	Q175H	NP_009083.2
XM_006718306.1	1260	Missense Mutation	CAA,CAC	Q190H	XP_006718369.1
XM_011520350.2	1260	Missense Mutation	CAA,CAC	Q251H	XP_011518652.1
XM_011520351.2	1260	Missense Mutation	CAA,CAC	Q251H	XP_011518653.1
XM_011520352.2	1260	Missense Mutation	CAA,CAC	Q213H	XP_011518654.1
XM_011520354.2	1260	Intron			XP_011518656.2
XM_017018260.1	1260	Missense Mutation	CAA,CAC	Q262H	XP_016873749.1
XM_017018261.1	1260	Missense Mutation	CAA,CAC	Q251H	XP_016873750.1
XM_017018262.1	1260	Missense Mutation	CAA,CAC	Q239H	XP_016873751.1
XM_017018263.1	1260	Missense Mutation	CAA,CAC	Q228H	XP_016873752.1
XM_017018264.1	1260	Missense Mutation	CAA,CAC	Q107H	XP_016873753.1
XM_017018265.1	1260	Missense Mutation	CAA,CAC	Q148H	XP_016873754.1
XM_017018266.1	1260	Missense Mutation	CAA,CAC	Q148H	XP_016873755.1
XM_017018267.1	1260	Missense Mutation	CAA,CAC	Q171H	XP_016873756.1

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