rs2126083898 Rat Genome Database

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Variant: rs2126083898 -  Homo sapiens

RGD ID: 153348948
RS ID: rs2126083898
ClinVar ID: CV1693017
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: FAT4  
Reference Nucleotide: A
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 4 126,398,492
GRCh38 4 125,477,337
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NG_033865.1:g.165926A>G
NC_000004.11:g.126398492A>G
NM_001291285.3:c.12479+3A>G
NM_001291303.3:c.12479+3A>G
More... 		12/26/2024 intron variant likely pathogenic|uncertain significance
Disease Annotations     Click to see Annotation Detail View


Variant Details
Variant Transcripts
Gene Symbol:FAT4
Accession:NM_024582
Location:INTRON

Gene Symbol:FAT4
Accession:NM_001291303
Location:INTRON

Gene Symbol:FAT4
Accession:NM_001291285
Location:INTRON

Gene Symbol:FAT4
Accession:XM_011532237
Location:INTRON

Gene Symbol:FAT4
Accession:XM_047416151
Location:INTRON

Gene Symbol:FAT4
Accession:XM_047416153
Location:INTRON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV002274857 CLINVAR
dbSNP (RS) rs2126083898 CLINVAR
MedGen C4014939 CLINVAR
NCBI Gene FAT4 CLINVAR
OMIM 612411 CLINVAR
  616006 CLINVAR