Product Details

SNP ID

rs139198011

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.11:3359334 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TGGTAATGTCTGAGAACCACATGAA[C/G]ACTCTGCCACATTCTTCACACTTGT

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	2193	Silent Mutation	GTC,GTG	V535V	NP_001123991.1
NM_001130520.2	2193	Silent Mutation	GTC,GTG	V558V	NP_001123992.1
NM_001242841.1	2193	Silent Mutation	GTC,GTG	V539V	NP_001229770.1
NM_001242842.1	2193	Silent Mutation	GTC,GTG	V513V	NP_001229771.1
NM_001242843.1	2193	Silent Mutation	GTC,GTG	V490V	NP_001229772.1
NM_001256823.1	2193	UTR 3			NP_001243752.1
NM_001256824.1	2193	Silent Mutation	GTC,GTG	V521V	NP_001243753.1
NM_001256825.1	2193	Silent Mutation	GTC,GTG	V490V	NP_001243754.1
NM_007152.4	2193	Silent Mutation	GTC,GTG	V486V	NP_009083.2
XM_006718306.1	2193	Silent Mutation	GTC,GTG	V501V	XP_006718369.1
XM_011520350.2	2193	Silent Mutation	GTC,GTG	V562V	XP_011518652.1
XM_011520351.2	2193	Silent Mutation	GTC,GTG	V562V	XP_011518653.1
XM_011520352.2	2193	Silent Mutation	GTC,GTG	V524V	XP_011518654.1
XM_011520354.2	2193	Intron			XP_011518656.2
XM_017018260.1	2193	Silent Mutation	GTC,GTG	V573V	XP_016873749.1
XM_017018261.1	2193	Silent Mutation	GTC,GTG	V562V	XP_016873750.1
XM_017018262.1	2193	Silent Mutation	GTC,GTG	V550V	XP_016873751.1
XM_017018263.1	2193	Silent Mutation	GTC,GTG	V539V	XP_016873752.1
XM_017018264.1	2193	Silent Mutation	GTC,GTG	V418V	XP_016873753.1
XM_017018265.1	2193	Silent Mutation	GTC,GTG	V459V	XP_016873754.1
XM_017018266.1	2193	Silent Mutation	GTC,GTG	V459V	XP_016873755.1
XM_017018267.1	2193	Silent Mutation	GTC,GTG	V482V	XP_016873756.1

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