RGD:11606101 Rat Genome Database

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Variant: RGD:11606101 -  Homo sapiens

RGD ID: 11606101
RS ID: rs542335688
ClinVar ID: CV323213
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: FAS  
Reference Nucleotide: T
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 10 90,774,789
GRCh38 10 89,015,032
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Age of Onset Trait Synonyms
LRG_134:g.29502T>G
NG_009089.2:g.29502T>G
NC_000010.11:g.89015032T>G
NC_000010.10:g.90774789T>G
More... 		01/13/2018 3 prime utr variant benign|likely benign all ages Autoimmune lymphoproliferative syndrome type 1, autosomal dominant; AUTOIMMUNE LYMPHOPROLIFERATIVE SYNDROME, TYPE I, AUTOSOMAL DOMINANT
Disease Annotations     Click to see Annotation Detail View


Variant Details
Variant Transcripts
Gene Symbol:FAS
Accession:XM_006717819
Location:3UTRS;EXON

Gene Symbol:FAS
Accession:XM_011539765
Location:3UTRS;EXON

Gene Symbol:FAS
Accession:XM_011539766
Location:3UTRS;EXON

Gene Symbol:FAS
Accession:NM_000043
Location:3UTRS;EXON

Gene Symbol:FAS
Accession:NM_152872
Location:3UTRS;EXON

Gene Symbol:
Accession:
Location:3UTRS;EXON

Gene Symbol:FAS
Accession:NM_001410956
Location:3UTRS;EXON

Gene Symbol:FAS
Accession:XM_011539764
Location:3UTRS;EXON

Gene Symbol:FAS
Accession:XM_047425178
Location:3UTRS;EXON

Gene Symbol:FAS
Accession:NM_001320619
Location:3UTRS;EXON

Gene Symbol:FAS
Accession:NM_152871
Location:3UTRS;EXON

Gene Symbol:FAS
Accession:NR_028035
Location:EXON;NON-CODING

Gene Symbol:FAS
Accession:NR_135314
Location:EXON;NON-CODING

Gene Symbol:FAS
Accession:NR_028033
Location:EXON;NON-CODING

Gene Symbol:FAS
Accession:NR_028034
Location:EXON;NON-CODING

Gene Symbol:FAS
Accession:NR_135315
Location:EXON;NON-CODING

Gene Symbol:FAS
Accession:NR_135313
Location:EXON;NON-CODING

Gene Symbol:FAS
Accession:NR_028036
Location:EXON;NON-CODING

Gene Symbol:FAS
Accession:XM_047425179
Location:INTRON

Gene Symbol:FAS
Accession:XM_047425180
Location:INTRON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV000327464 CLINVAR
dbSNP (RS) rs542335688 CLINVAR
MedGen C1328840 CLINVAR
NCBI Gene FAS CLINVAR
OMIM 134637 CLINVAR
  601859 CLINVAR