RGD:38597924 Rat Genome Database

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Variant: RGD:38597924 -  Homo sapiens

RGD ID: 38597924
RS ID: rs759743352
ClinVar ID: CV861318
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: HRAS  LOC127819987  LRRC56  
Reference Nucleotide: G
Variant Nucleotide: C
Position
Assembly Chr Position
GRCh37 11 534,194
GRCh38 11 534,194
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_001130442.3:c.111+18G>C
NM_176795.5:c.111+18G>C
NM_001318054.2:c.-209+18G>C
NM_001130442.2:c.111+18G>C
More... 		05/05/2020 intron variant uncertain significance Lung cancer, squamous cell, somatic; Squamous cell carcinoma of lung
Disease Annotations     Click to see Annotation Detail View

Phenotype Annotations     Click to see Annotation Detail View

Human Phenotype

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

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

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

Gene Symbol:LRRC56
Accession:XM_017017167
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_005252776
Location:INTRON

Gene Symbol:LRRC56
Accession:XM_006718133
Location:INTRON

Gene Symbol:LRRC56
Accession:XM_005252775
Location:INTRON

Gene Symbol:LRRC56
Accession:XM_006718132
Location:INTRON

Gene Symbol:LRRC56
Accession:XM_011519876
Location:INTRON

Gene Symbol:HRAS
Accession:NM_001130442
Location:INTRON

Gene Symbol:HRAS
Accession:NM_176795
Location:INTRON

Gene Symbol:LRRC56
Accession:NM_198075
Location:INTRON

Gene Symbol:HRAS
Accession:NM_005343
Location:INTRON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV001250981 CLINVAR
dbSNP (RS) rs759743352 CLINVAR
MedGen C0149782 CLINVAR
NCBI Gene HRAS CLINVAR
  LRRC56 CLINVAR
OMIM 190020 CLINVAR
  618227 CLINVAR