RGD:150481875 Rat Genome Database

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Variant: RGD:150481875 -  Homo sapiens

RGD ID: 150481875
RS ID: rs11370544
ClinVar ID: CV1279852
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: FADD  
Reference Nucleotide: -
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 11 70,052,077
GRCh38 11 70,205,971
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_003824.4:c.287-162_287-161insA
LRG_228:g.7809_7810insA
NG_027966.1:g.7809_7810insA
NC_000011.10:g.70205971_70205972insA
More... 		05/11/2021 intron variant benign none provided

Variant Details
Variant Transcripts
Gene Symbol:FADD
Accession:NM_003824
Location:INTRON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV001714925 CLINVAR
dbSNP (RS) rs11370544 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene FADD CLINVAR
OMIM 602457 CLINVAR