RGD:28878185 Rat Genome Database

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Variant: RGD:28878185 -  Homo sapiens

RGD ID: 28878185
RS ID: rs146143405
ClinVar ID: CV890268
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: FGG  
Reference Nucleotide: T
Variant Nucleotide: C
Position
Assembly Chr Position
GRCh37 4 155,525,451
GRCh38 4 154,604,299
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_021870.3:c.*535A>G
NG_008834.1:g.13452A>G
NC_000004.12:g.154604299T>C
NC_000004.11:g.155525451T>C
More... 		01/13/2018 3 prime utr variant likely benign
Disease Annotations     Click to see Annotation Detail View


Variant Details
Variant Transcripts
Gene Symbol:FGG
Accession:NM_000509
Location:3UTRS;EXON

Gene Symbol:FGG
Accession:NM_021870
Location:3UTRS;EXON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV001148601 CLINVAR
dbSNP (RS) rs146143405 CLINVAR
MedGen C2584774 CLINVAR
NCBI Gene FGG CLINVAR
OMIM 134850 CLINVAR
  202400 CLINVAR