Product Details

SNP ID

rs138087772

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.19:43913585 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

ATGAGCTCCAGCTGAAGACTTTCCC[A/G]CATTCCTCACATTTGTATGGTCTCT

Phenotype

MIM: 194554

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

ZNF45 PubMed Links

Gene Details

Gene

ZNF45

Gene Name

zinc finger protein 45

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_003425.3	3005	Silent Mutation	TGC,TGT	C617C	NP_003416.1
XM_011527267.1	3005	Silent Mutation	TGC,TGT	C617C	XP_011525569.1
XM_011527269.1	3005	Silent Mutation	TGC,TGT	C617C	XP_011525571.1
XM_011527271.1	3005	Silent Mutation	TGC,TGT	C617C	XP_011525573.1
XM_011527273.1	3005	Silent Mutation	TGC,TGT	C617C	XP_011525575.1
XM_017027217.1	3005	Silent Mutation	TGC,TGT	C617C	XP_016882706.1
XM_017027218.1	3005	Silent Mutation	TGC,TGT	C617C	XP_016882707.1
XM_017027219.1	3005	Silent Mutation	TGC,TGT	C617C	XP_016882708.1
XM_017027220.1	3005	Silent Mutation	TGC,TGT	C617C	XP_016882709.1
XM_017027221.1	3005	Silent Mutation	TGC,TGT	C617C	XP_016882710.1
XM_017027222.1	3005	Silent Mutation	TGC,TGT	C617C	XP_016882711.1
XM_017027223.1	3005	Silent Mutation	TGC,TGT	C617C	XP_016882712.1
XM_017027224.1	3005	Silent Mutation	TGC,TGT	C617C	XP_016882713.1
XM_017027225.1	3005	Silent Mutation	TGC,TGT	C617C	XP_016882714.1
XM_017027226.1	3005	Silent Mutation	TGC,TGT	C617C	XP_016882715.1
XM_017027227.1	3005	Silent Mutation	TGC,TGT	C617C	XP_016882716.1
XM_017027228.1	3005	Silent Mutation	TGC,TGT	C581C	XP_016882717.1
XM_017027229.1	3005	Silent Mutation	TGC,TGT	C581C	XP_016882718.1
XM_017027230.1	3005	Silent Mutation	TGC,TGT	C581C	XP_016882719.1

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