RGD:11625367 Rat Genome Database

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Variant: RGD:11625367 -  Homo sapiens

RGD ID: 11625367
RS ID: rs57161046
ClinVar ID: CV330024
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: LOC127887971  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 17 73,840,668
GRCh38 17 75,844,587
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
LRG_122t1:c.-250C>T
LRG_122:g.5131C>T
NG_007266.1:g.5131C>T
NC_000017.11:g.75844587G>A
More... 		01/13/2018 5 prime utr variant benign|likely benign
Disease Annotations     Click to see Annotation Detail View


Variant Details
Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV000398080 CLINVAR
dbSNP (RS) rs57161046 CLINVAR
MedGen C1837174 CLINVAR
NCBI Gene UNC13D CLINVAR
OMIM 608897 CLINVAR
  608898 CLINVAR