Product Details

SNP ID

rs199638490

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.19:43913730 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GACTCCACGATGTGCCAGAAAATTG[C/G]AGGCCCGACAGAAGCCCTTCCCACA

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	2860	Missense Mutation	TCC,TGC	S569C	NP_003416.1
XM_011527267.1	2860	Missense Mutation	TCC,TGC	S569C	XP_011525569.1
XM_011527269.1	2860	Missense Mutation	TCC,TGC	S569C	XP_011525571.1
XM_011527271.1	2860	Missense Mutation	TCC,TGC	S569C	XP_011525573.1
XM_011527273.1	2860	Missense Mutation	TCC,TGC	S569C	XP_011525575.1
XM_017027217.1	2860	Missense Mutation	TCC,TGC	S569C	XP_016882706.1
XM_017027218.1	2860	Missense Mutation	TCC,TGC	S569C	XP_016882707.1
XM_017027219.1	2860	Missense Mutation	TCC,TGC	S569C	XP_016882708.1
XM_017027220.1	2860	Missense Mutation	TCC,TGC	S569C	XP_016882709.1
XM_017027221.1	2860	Missense Mutation	TCC,TGC	S569C	XP_016882710.1
XM_017027222.1	2860	Missense Mutation	TCC,TGC	S569C	XP_016882711.1
XM_017027223.1	2860	Missense Mutation	TCC,TGC	S569C	XP_016882712.1
XM_017027224.1	2860	Missense Mutation	TCC,TGC	S569C	XP_016882713.1
XM_017027225.1	2860	Missense Mutation	TCC,TGC	S569C	XP_016882714.1
XM_017027226.1	2860	Missense Mutation	TCC,TGC	S569C	XP_016882715.1
XM_017027227.1	2860	Missense Mutation	TCC,TGC	S569C	XP_016882716.1
XM_017027228.1	2860	Missense Mutation	TCC,TGC	S533C	XP_016882717.1
XM_017027229.1	2860	Missense Mutation	TCC,TGC	S533C	XP_016882718.1
XM_017027230.1	2860	Missense Mutation	TCC,TGC	S533C	XP_016882719.1

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