Product Details

SNP ID

rs202013490

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.19:53068462 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GTGAGTCCTTTGATGATTTGCAAGG[C/T]GTGAGTTCTGAGTGAAGACCTTGCC

Phenotype

MIM: 600398

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

ZNF160 PubMed Links

Gene Details

Gene

ZNF160

Gene Name

zinc finger protein 160

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001102603.1	2484	Missense Mutation	CAC,CGC	H691R	NP_001096073.1
NM_001322125.1	2484	Intron			NP_001309054.1
NM_001322126.1	2484	Intron			NP_001309055.1
NM_001322128.1	2484	Missense Mutation	CAC,CGC	H691R	NP_001309057.1
NM_001322129.1	2484	Missense Mutation	CAC,CGC	H691R	NP_001309058.1
NM_001322130.1	2484	Missense Mutation	CAC,CGC	H691R	NP_001309059.1
NM_001322131.1	2484	Missense Mutation	CAC,CGC	H691R	NP_001309060.1
NM_001322132.1	2484	Missense Mutation	CAC,CGC	H691R	NP_001309061.1
NM_001322133.1	2484	Missense Mutation	CAC,CGC	H691R	NP_001309062.1
NM_001322134.1	2484	Missense Mutation	CAC,CGC	H691R	NP_001309063.1
NM_001322135.1	2484	Missense Mutation	CAC,CGC	H691R	NP_001309064.1
NM_001322136.1	2484	Missense Mutation	CAC,CGC	H691R	NP_001309065.1
NM_001322137.1	2484	Missense Mutation	CAC,CGC	H655R	NP_001309066.1
NM_001322138.1	2484	Missense Mutation	CAC,CGC	H655R	NP_001309067.1
NM_001322139.1	2484	Missense Mutation	CAC,CGC	H655R	NP_001309068.1
NM_033288.3	2484	Missense Mutation	CAC,CGC	H691R	NP_150630.2
NM_198893.2	2484	Missense Mutation	CAC,CGC	H691R	NP_942596.1
XM_017027445.1	2484	Missense Mutation	CAC,CGC	H710R	XP_016882934.1
XM_017027446.1	2484	Missense Mutation	CAC,CGC	H691R	XP_016882935.1
XM_017027447.1	2484	Intron			XP_016882936.1
XM_017027448.1	2484	Intron			XP_016882937.1

View Full Product Details