Product Details

SNP ID

rs201516625

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.19:43913535 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

ACATTTGTATGGTTTTTCTCCGGTG[C/T]GAACTCTTTGATGGGCTTGAAGGTA

Phenotype

MIM: 194554

Polymorphism

C/T, 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	3055	Missense Mutation	CAC,CGC	H634R	NP_003416.1
XM_011527267.1	3055	Missense Mutation	CAC,CGC	H634R	XP_011525569.1
XM_011527269.1	3055	Missense Mutation	CAC,CGC	H634R	XP_011525571.1
XM_011527271.1	3055	Missense Mutation	CAC,CGC	H634R	XP_011525573.1
XM_011527273.1	3055	Missense Mutation	CAC,CGC	H634R	XP_011525575.1
XM_017027217.1	3055	Missense Mutation	CAC,CGC	H634R	XP_016882706.1
XM_017027218.1	3055	Missense Mutation	CAC,CGC	H634R	XP_016882707.1
XM_017027219.1	3055	Missense Mutation	CAC,CGC	H634R	XP_016882708.1
XM_017027220.1	3055	Missense Mutation	CAC,CGC	H634R	XP_016882709.1
XM_017027221.1	3055	Missense Mutation	CAC,CGC	H634R	XP_016882710.1
XM_017027222.1	3055	Missense Mutation	CAC,CGC	H634R	XP_016882711.1
XM_017027223.1	3055	Missense Mutation	CAC,CGC	H634R	XP_016882712.1
XM_017027224.1	3055	Missense Mutation	CAC,CGC	H634R	XP_016882713.1
XM_017027225.1	3055	Missense Mutation	CAC,CGC	H634R	XP_016882714.1
XM_017027226.1	3055	Missense Mutation	CAC,CGC	H634R	XP_016882715.1
XM_017027227.1	3055	Missense Mutation	CAC,CGC	H634R	XP_016882716.1
XM_017027228.1	3055	Missense Mutation	CAC,CGC	H598R	XP_016882717.1
XM_017027229.1	3055	Missense Mutation	CAC,CGC	H598R	XP_016882718.1
XM_017027230.1	3055	Missense Mutation	CAC,CGC	H598R	XP_016882719.1

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