Product Details

SNP ID

rs141747981

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.11:3359490 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TTTTCTTATGCTTAGTGAGGTCTGA[C/T]AACTGCTTAAAGATGTTGCCACATT

Phenotype

MIM: 602187

Polymorphism

C/T, Transition 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	2037	Silent Mutation	TTA,TTG	L483L	NP_001123991.1
NM_001130520.2	2037	Silent Mutation	TTA,TTG	L506L	NP_001123992.1
NM_001242841.1	2037	Silent Mutation	TTA,TTG	L487L	NP_001229770.1
NM_001242842.1	2037	Silent Mutation	TTA,TTG	L461L	NP_001229771.1
NM_001242843.1	2037	Silent Mutation	TTA,TTG	L438L	NP_001229772.1
NM_001256823.1	2037	UTR 3			NP_001243752.1
NM_001256824.1	2037	Silent Mutation	TTA,TTG	L469L	NP_001243753.1
NM_001256825.1	2037	Silent Mutation	TTA,TTG	L438L	NP_001243754.1
NM_007152.4	2037	Silent Mutation	TTA,TTG	L434L	NP_009083.2
XM_006718306.1	2037	Silent Mutation	TTA,TTG	L449L	XP_006718369.1
XM_011520350.2	2037	Silent Mutation	TTA,TTG	L510L	XP_011518652.1
XM_011520351.2	2037	Silent Mutation	TTA,TTG	L510L	XP_011518653.1
XM_011520352.2	2037	Silent Mutation	TTA,TTG	L472L	XP_011518654.1
XM_011520354.2	2037	Intron			XP_011518656.2
XM_017018260.1	2037	Silent Mutation	TTA,TTG	L521L	XP_016873749.1
XM_017018261.1	2037	Silent Mutation	TTA,TTG	L510L	XP_016873750.1
XM_017018262.1	2037	Silent Mutation	TTA,TTG	L498L	XP_016873751.1
XM_017018263.1	2037	Silent Mutation	TTA,TTG	L487L	XP_016873752.1
XM_017018264.1	2037	Silent Mutation	TTA,TTG	L366L	XP_016873753.1
XM_017018265.1	2037	Silent Mutation	TTA,TTG	L407L	XP_016873754.1
XM_017018266.1	2037	Silent Mutation	TTA,TTG	L407L	XP_016873755.1
XM_017018267.1	2037	Silent Mutation	TTA,TTG	L430L	XP_016873756.1

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