RGD:11659250 Rat Genome Database

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Variant: RGD:11659250 -  Homo sapiens

RGD ID: 11659250
RS ID: rs886052820
ClinVar ID: CV345517
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: LOC130060715  RAD51D  RAD51L3-RFFL  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 17 33,446,771
GRCh38 17 35,119,752
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
LRG_516:g.5118C>T
NG_031858.1:g.5118C>T
NC_000017.11:g.35119752G>A
NC_000017.10:g.33446771G>A
More...
06/14/2016 5 prime utr variant uncertain significance
Disease Annotations     Click to see Annotation Detail View


Variant Details
Variant Transcripts
Gene Symbol:RAD51D
Accession:NM_133629
Location:5UTRS;EXON

Gene Symbol:RAD51D
Accession:NM_001142571
Location:5UTRS;EXON

Gene Symbol:RAD51D
Accession:NM_002878
Location:5UTRS;EXON

Gene Symbol:RAD51D
Accession:NR_037712
Location:EXON;NON-CODING

Gene Symbol:RAD51D
Accession:NR_037711
Location:EXON;NON-CODING

Gene Symbol:RAD51L3-RFFL
Accession:NR_037714
Location:INTRON;NON-CODING

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV000356343 CLINVAR
dbSNP (RS) rs886052820 CLINVAR
MedGen CN239207 CLINVAR
NCBI Gene 100529207 CLINVAR
  LOC130060715 CLINVAR
  RAD51D CLINVAR
OMIM 602954 CLINVAR