Product Details

SNP ID

rs149151185

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.19:43913448 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

AAAGTCCTTGTCACCCTCATCATCA[A/G]CATGGACTCGCTGATGAATGATAAG

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	3142	Missense Mutation	GCT,GTT	A663V	NP_003416.1
XM_011527267.1	3142	Missense Mutation	GCT,GTT	A663V	XP_011525569.1
XM_011527269.1	3142	Missense Mutation	GCT,GTT	A663V	XP_011525571.1
XM_011527271.1	3142	Missense Mutation	GCT,GTT	A663V	XP_011525573.1
XM_011527273.1	3142	Missense Mutation	GCT,GTT	A663V	XP_011525575.1
XM_017027217.1	3142	Missense Mutation	GCT,GTT	A663V	XP_016882706.1
XM_017027218.1	3142	Missense Mutation	GCT,GTT	A663V	XP_016882707.1
XM_017027219.1	3142	Missense Mutation	GCT,GTT	A663V	XP_016882708.1
XM_017027220.1	3142	Missense Mutation	GCT,GTT	A663V	XP_016882709.1
XM_017027221.1	3142	Missense Mutation	GCT,GTT	A663V	XP_016882710.1
XM_017027222.1	3142	Missense Mutation	GCT,GTT	A663V	XP_016882711.1
XM_017027223.1	3142	Missense Mutation	GCT,GTT	A663V	XP_016882712.1
XM_017027224.1	3142	Missense Mutation	GCT,GTT	A663V	XP_016882713.1
XM_017027225.1	3142	Missense Mutation	GCT,GTT	A663V	XP_016882714.1
XM_017027226.1	3142	Missense Mutation	GCT,GTT	A663V	XP_016882715.1
XM_017027227.1	3142	Missense Mutation	GCT,GTT	A663V	XP_016882716.1
XM_017027228.1	3142	Missense Mutation	GCT,GTT	A627V	XP_016882717.1
XM_017027229.1	3142	Missense Mutation	GCT,GTT	A627V	XP_016882718.1
XM_017027230.1	3142	Missense Mutation	GCT,GTT	A627V	XP_016882719.1

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