Product Details

SNP ID

rs62619253

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.11:3360139 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TTTCTCTCCAGTGTCAATGTTCTCA[C/G]GTTCAGTAAAGTGTGAGCACTGGAT

Phenotype

MIM: 602187

Polymorphism

C/G, 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	1388	Missense Mutation	CCT,CGT	P267R	NP_001123991.1
NM_001130520.2	1388	Missense Mutation	CCT,CGT	P290R	NP_001123992.1
NM_001242841.1	1388	Missense Mutation	CCT,CGT	P271R	NP_001229770.1
NM_001242842.1	1388	Missense Mutation	CCT,CGT	P245R	NP_001229771.1
NM_001242843.1	1388	Missense Mutation	CCT,CGT	P222R	NP_001229772.1
NM_001256823.1	1388	UTR 3			NP_001243752.1
NM_001256824.1	1388	Missense Mutation	CCT,CGT	P253R	NP_001243753.1
NM_001256825.1	1388	Missense Mutation	CCT,CGT	P222R	NP_001243754.1
NM_007152.4	1388	Missense Mutation	CCT,CGT	P218R	NP_009083.2
XM_006718306.1	1388	Missense Mutation	CCT,CGT	P233R	XP_006718369.1
XM_011520350.2	1388	Missense Mutation	CCT,CGT	P294R	XP_011518652.1
XM_011520351.2	1388	Missense Mutation	CCT,CGT	P294R	XP_011518653.1
XM_011520352.2	1388	Missense Mutation	CCT,CGT	P256R	XP_011518654.1
XM_011520354.2	1388	Intron			XP_011518656.2
XM_017018260.1	1388	Missense Mutation	CCT,CGT	P305R	XP_016873749.1
XM_017018261.1	1388	Missense Mutation	CCT,CGT	P294R	XP_016873750.1
XM_017018262.1	1388	Missense Mutation	CCT,CGT	P282R	XP_016873751.1
XM_017018263.1	1388	Missense Mutation	CCT,CGT	P271R	XP_016873752.1
XM_017018264.1	1388	Missense Mutation	CCT,CGT	P150R	XP_016873753.1
XM_017018265.1	1388	Missense Mutation	CCT,CGT	P191R	XP_016873754.1
XM_017018266.1	1388	Missense Mutation	CCT,CGT	P191R	XP_016873755.1
XM_017018267.1	1388	Missense Mutation	CCT,CGT	P214R	XP_016873756.1

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