Product Details

SNP ID

rs407731

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.19:43913925 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

GAACTGACTGAAGGCCTTACCACAC[C/T]TCTCGCATTTATAGGGTTTCTCTCC

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	2665	Missense Mutation	AAG,AGG	K504R	NP_003416.1
XM_011527267.1	2665	Missense Mutation	AAG,AGG	K504R	XP_011525569.1
XM_011527269.1	2665	Missense Mutation	AAG,AGG	K504R	XP_011525571.1
XM_011527271.1	2665	Missense Mutation	AAG,AGG	K504R	XP_011525573.1
XM_011527273.1	2665	Missense Mutation	AAG,AGG	K504R	XP_011525575.1
XM_017027217.1	2665	Missense Mutation	AAG,AGG	K504R	XP_016882706.1
XM_017027218.1	2665	Missense Mutation	AAG,AGG	K504R	XP_016882707.1
XM_017027219.1	2665	Missense Mutation	AAG,AGG	K504R	XP_016882708.1
XM_017027220.1	2665	Missense Mutation	AAG,AGG	K504R	XP_016882709.1
XM_017027221.1	2665	Missense Mutation	AAG,AGG	K504R	XP_016882710.1
XM_017027222.1	2665	Missense Mutation	AAG,AGG	K504R	XP_016882711.1
XM_017027223.1	2665	Missense Mutation	AAG,AGG	K504R	XP_016882712.1
XM_017027224.1	2665	Missense Mutation	AAG,AGG	K504R	XP_016882713.1
XM_017027225.1	2665	Missense Mutation	AAG,AGG	K504R	XP_016882714.1
XM_017027226.1	2665	Missense Mutation	AAG,AGG	K504R	XP_016882715.1
XM_017027227.1	2665	Missense Mutation	AAG,AGG	K504R	XP_016882716.1
XM_017027228.1	2665	Missense Mutation	AAG,AGG	K468R	XP_016882717.1
XM_017027229.1	2665	Missense Mutation	AAG,AGG	K468R	XP_016882718.1
XM_017027230.1	2665	Missense Mutation	AAG,AGG	K468R	XP_016882719.1

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