Product Details

SNP ID

rs145189460

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.19:43913437 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TCTGATGAAGGAAAGTCCTTGTCAC[C/G]CTCATCATCAGCATGGACTCGCTGA

Phenotype

MIM: 194554

Polymorphism

C/G, Transversion 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	3153	Missense Mutation	CGT,GGT	R667G	NP_003416.1
XM_011527267.1	3153	Missense Mutation	CGT,GGT	R667G	XP_011525569.1
XM_011527269.1	3153	Missense Mutation	CGT,GGT	R667G	XP_011525571.1
XM_011527271.1	3153	Missense Mutation	CGT,GGT	R667G	XP_011525573.1
XM_011527273.1	3153	Missense Mutation	CGT,GGT	R667G	XP_011525575.1
XM_017027217.1	3153	Missense Mutation	CGT,GGT	R667G	XP_016882706.1
XM_017027218.1	3153	Missense Mutation	CGT,GGT	R667G	XP_016882707.1
XM_017027219.1	3153	Missense Mutation	CGT,GGT	R667G	XP_016882708.1
XM_017027220.1	3153	Missense Mutation	CGT,GGT	R667G	XP_016882709.1
XM_017027221.1	3153	Missense Mutation	CGT,GGT	R667G	XP_016882710.1
XM_017027222.1	3153	Missense Mutation	CGT,GGT	R667G	XP_016882711.1
XM_017027223.1	3153	Missense Mutation	CGT,GGT	R667G	XP_016882712.1
XM_017027224.1	3153	Missense Mutation	CGT,GGT	R667G	XP_016882713.1
XM_017027225.1	3153	Missense Mutation	CGT,GGT	R667G	XP_016882714.1
XM_017027226.1	3153	Missense Mutation	CGT,GGT	R667G	XP_016882715.1
XM_017027227.1	3153	Missense Mutation	CGT,GGT	R667G	XP_016882716.1
XM_017027228.1	3153	Missense Mutation	CGT,GGT	R631G	XP_016882717.1
XM_017027229.1	3153	Missense Mutation	CGT,GGT	R631G	XP_016882718.1
XM_017027230.1	3153	Missense Mutation	CGT,GGT	R631G	XP_016882719.1

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