RGD:405175696 Rat Genome Database

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Variant: RGD:405175696 -  Homo sapiens

RGD ID: 405175696
ClinVar ID: CV2864618
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: GFM1  
Reference Nucleotide: -
Variant Nucleotide: C
Position
Assembly Chr Position
GRCh37 3 158,399,765
GRCh38 3 158,681,976
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_001374359.1:c.1035-19_1035-18insC
NM_001374360.1:c.1035-19_1035-18insC
NM_001374358.1:c.1143-19_1143-18insC
NM_001374357.1:c.1377-19_1377-18insC
More... 		11/14/2023 intron variant likely benign none provided

Variant Details
Variant Transcripts
Gene Symbol:GFM1
Accession:NM_024996
Location:INTRON

Gene Symbol:GFM1
Accession:NM_001374355
Location:INTRON

Gene Symbol:GFM1
Accession:NM_001374359
Location:INTRON

Gene Symbol:GFM1
Accession:NM_001374356
Location:INTRON

Gene Symbol:GFM1
Accession:NM_001308166
Location:INTRON

Gene Symbol:GFM1
Accession:NM_001374361
Location:INTRON

Gene Symbol:GFM1
Accession:NM_001374358
Location:INTRON

Gene Symbol:GFM1
Accession:NM_001374360
Location:INTRON

Gene Symbol:GFM1
Accession:NM_001374357
Location:INTRON

Gene Symbol:GFM1
Accession:NM_001308164
Location:INTRON

Gene Symbol:GFM1
Accession:NR_164500
Location:INTRON;NON-CODING

Gene Symbol:GFM1
Accession:NR_164501
Location:INTRON;NON-CODING

Gene Symbol:GFM1
Accession:NR_164499
Location:INTRON;NON-CODING

Gene Symbol:GFM1
Accession:NR_164502
Location:INTRON;NON-CODING

Variant Samples
Additional References at PubMed
PMID:28492532  


Additional Information

Database Acc Id Source(s)
ClinVar RCV003542738 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene GFM1 CLINVAR
OMIM 606639 CLINVAR