RGD:155267146 Rat Genome Database

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Variant: RGD:155267146 -  Homo sapiens

RGD ID: 155267146
ClinVar ID: CV1699452
Genic Status: GENIC
Type: insertion (SO:0000667) 
Associated Genes: DLAT  
Reference Nucleotide: -
Variant Nucleotide: TT
Position
Assembly Chr Position
GRCh37 11 111,897,029
GRCh38 11 112,026,305
JBrowse: View Region in Genome Browser (JBrowse)
Model



HGVS Name(s)
Last Evaluated
Molecular Consequence
Clinical Significance
Trait Synonyms
NM_001372038.1:c.381+21_381+22dup
NM_001372039.1:c.381+21_381+22dup
NM_001372041.1:c.381+21_381+22dup
NM_001931.5:c.381+21_381+22dup
More... 		03/08/2022 intron variant likely benign none provided

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Database
Acc Id
Source(s)
ClinVar RCV002283247 CLINVAR
MedGen CN517202 CLINVAR
NCBI Gene DLAT CLINVAR
OMIM 608770 CLINVAR