RGD:407463111 Rat Genome Database

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Variant: RGD:407463111 -  Homo sapiens

RGD ID: 407463111
ClinVar ID: CV3488608
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: ZNF22  
Reference Nucleotide: G
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 10 45,498,841
GRCh38 10 45,003,393
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_006963.5:c.25G>T
NC_000010.11:g.45003393G>T
NC_000010.10:g.45498841G>T
NM_006963.4:c.25G>T
More... 		03/15/2024 missense variant uncertain significance AllHighlyPenetrant

Variant Details
Variant Transcripts
Gene Symbol:ZNF22
Accession:NM_006963
Location:EXON
Amino Acid Prediction: G to C (nonsynonymous)
Amino Acid Position: 9
Amino Acid Sequence
(Calculated using NCBI transcript definition)
MRLAKPKACISRSSSQGKAYENKRKTGRQRQKWGMTIRFDSSFSRLRRSLDDKPYKCTECEKSFSQSSTLFQHQKIHTGK
KSHKCADCGKSFFQSSNLIQHRRIHTGEKPYKCDECGESFKQSSNLIQHQRIHTGEKPYQCDECGRCFSQSSHLIQHQRT
HTGEKPYQCSECGKCFSQSSHLRQHMKVHKEEKPRKTRGKNIRVKTHLPSWKAGTGRKSVAGLR*
.
Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV004688171 CLINVAR
MedGen CN169374 CLINVAR
NCBI Gene ZNF22 CLINVAR
OMIM 194529 CLINVAR