RGD:8644236 Rat Genome Database

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Variant: RGD:8644236 -  Homo sapiens

RGD ID: 8644236
RS ID: rs104895281
ClinVar ID: CV103584
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: TNFRSF1A  
Reference Nucleotide: T
Variant Nucleotide: C
Position
Assembly Chr Position
GRCh37 12 6,442,714
GRCh38 12 6,333,548
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_193:g.13548A>G
NG_007506.1:g.13548A>G
NC_000012.12:g.6333548T>C
NC_000012.11:g.6442714T>C
More... 		intron|intron variant not provided adolescent|childhood|infancy Autosomal Dominant Familial Periodic Fever; Familial Hibernian fever; TNF receptor-associated periodic syndrome; Tumor necrosis factor receptor-associated periodic syndrome

Variant Details
Variant Transcripts
Gene Symbol:TNFRSF1A
Accession:NM_001346092
Location:5UTRS;INTRON

Gene Symbol:TNFRSF1A
Accession:NM_001346091
Location:5UTRS;INTRON

Gene Symbol:TNFRSF1A
Accession:NM_001065
Location:INTRON

Gene Symbol:TNFRSF1A
Accession:NR_144351
Location:INTRON;NON-CODING

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV000083945 CLINVAR
dbSNP (RS) rs104895281 CLINVAR
MedGen C1275126 CLINVAR
NCBI Gene TNFRSF1A CLINVAR
OMIM 142680 CLINVAR
  191190 CLINVAR
SNOMED CT 403833009 CLINVAR