RGD:407466383 Rat Genome Database

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Variant: RGD:407466383 -  Homo sapiens

RGD ID: 407466383
ClinVar ID: CV3440614
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: IFNL3  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 19 39,734,783
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
LRG_1011t1:c.285C>T
NM_172139.4:c.273C>T
NM_001346937.2:c.285C>T
LRG_1011:g.5829C>T
More...
03/26/2024 synonymous variant likely benign AllHighlyPenetrant

Variant Details
Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV004635617 CLINVAR
MedGen CN169374 CLINVAR
NCBI Gene IFNL3 CLINVAR
OMIM 607402 CLINVAR