RGD:152038875 Rat Genome Database

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Variant: RGD:152038875 -  Homo sapiens

RGD ID: 152038875
RS ID: rs779917193
ClinVar ID: CV1647858
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: HRAS  LRRC56  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 11 533,628
GRCh38 11 533,628
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
LRG_506t1:c.291-16G>A
NM_001318054.2:c.-29-16G>A
NM_001130442.3:c.291-16G>A
NM_005343.4:c.291-16G>A
More... 		06/15/2021 intron variant likely benign Faciocutaneoskeletal syndrome; FCS syndrome
Disease Annotations     Click to see Annotation Detail View


Variant Details
Variant Transcripts
Gene Symbol:HRAS
Accession:NM_001318054
Location:5UTRS;INTRON

Gene Symbol:LRRC56
Accession:XM_011519877
Location:5UTRS;INTRON

Gene Symbol:LRRC56
Accession:XM_047426336
Location:5UTRS;INTRON

Gene Symbol:LRRC56
Accession:XM_017017167
Location:5UTRS;INTRON

Gene Symbol:LRRC56
Accession:XM_011519875
Location:5UTRS;INTRON

Gene Symbol:LRRC56
Accession:XM_017017168
Location:5UTRS;INTRON

Gene Symbol:HRAS
Accession:NM_001130442
Location:INTRON

Gene Symbol:LRRC56
Accession:XM_006718133
Location:INTRON

Gene Symbol:HRAS
Accession:NM_176795
Location:INTRON

Gene Symbol:HRAS
Accession:NM_005343
Location:INTRON

Gene Symbol:LRRC56
Accession:XM_005252775
Location:INTRON

Gene Symbol:LRRC56
Accession:XM_006718132
Location:INTRON

Gene Symbol:LRRC56
Accession:NM_198075
Location:INTRON

Gene Symbol:LRRC56
Accession:XM_005252776
Location:INTRON

Gene Symbol:LRRC56
Accession:XM_011519876
Location:INTRON

Variant Samples
Additional References at PubMed
PMID:28492532  


Additional Information

Database Acc Id Source(s)
ClinVar RCV002087656 CLINVAR
dbSNP (RS) rs779917193 CLINVAR
MedGen C0587248 CLINVAR
NCBI Gene HRAS CLINVAR
  LRRC56 CLINVAR
OMIM 190020 CLINVAR
  218040 CLINVAR
  618227 CLINVAR
SNOMED CT 309776008 CLINVAR