RGD:14745347 Rat Genome Database

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Variant: RGD:14745347 -  Homo sapiens

RGD ID: 14745347
RS ID: rs1588873485
ClinVar ID: CV652000
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: RET  
Reference Nucleotide: T
Variant Nucleotide: C
Position
Assembly Chr Position
GRCh37 10 43,609,129
GRCh38 10 43,113,681
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
LRG_518t1:c.1879+6T>C
NM_020975.6:c.1879+6T>C
LRG_518:g.41613T>C
NG_007489.1:g.41613T>C
More... 		11/09/2018 intron variant uncertain significance
Disease Annotations     Click to see Annotation Detail View


Variant Details
Variant Transcripts
Gene Symbol:RET
Accession:NM_001406744
Location:INTRON

Gene Symbol:RET
Accession:NM_001406763
Location:INTRON

Gene Symbol:RET
Accession:NM_001406743
Location:INTRON

Gene Symbol:RET
Accession:NM_001406780
Location:INTRON

Gene Symbol:RET
Accession:NM_001406779
Location:INTRON

Gene Symbol:RET
Accession:NM_020975
Location:INTRON

Gene Symbol:RET
Accession:NM_001406764
Location:INTRON

Gene Symbol:RET
Accession:NM_001406760
Location:INTRON

Gene Symbol:RET
Accession:NM_001406759
Location:INTRON

Gene Symbol:RET
Accession:NM_001406768
Location:INTRON

Gene Symbol:RET
Accession:NM_020630
Location:INTRON

Gene Symbol:RET
Accession:NM_001406773
Location:INTRON

Gene Symbol:RET
Accession:NM_001355216
Location:INTRON

Gene Symbol:RET
Accession:NM_001406775
Location:INTRON

Gene Symbol:RET
Accession:NM_001406776
Location:INTRON

Gene Symbol:RET
Accession:NM_001406789
Location:INTRON

Gene Symbol:RET
Accession:NM_001406791
Location:INTRON

Gene Symbol:RET
Accession:NM_001406784
Location:INTRON

Gene Symbol:RET
Accession:NM_001406793
Location:INTRON

Gene Symbol:RET
Accession:NM_001406765
Location:INTRON

Gene Symbol:RET
Accession:NM_001406782
Location:INTRON

Gene Symbol:RET
Accession:NM_001406787
Location:INTRON

Gene Symbol:RET
Accession:NM_001406767
Location:INTRON

Gene Symbol:RET
Accession:NM_001406778
Location:INTRON

Gene Symbol:RET
Accession:NM_001406788
Location:INTRON

Gene Symbol:RET
Accession:NM_001406762
Location:INTRON

Gene Symbol:RET
Accession:NM_001406761
Location:INTRON

Gene Symbol:RET
Accession:NM_001406774
Location:INTRON

Gene Symbol:RET
Accession:NM_001406783
Location:INTRON

Gene Symbol:RET
Accession:NM_001406769
Location:INTRON

Gene Symbol:RET
Accession:NM_001406766
Location:INTRON

Gene Symbol:RET
Accession:NM_001406794
Location:INTRON

Gene Symbol:RET
Accession:NM_001406772
Location:INTRON

Gene Symbol:RET
Accession:NM_001406771
Location:INTRON

Gene Symbol:RET
Accession:NM_001406785
Location:INTRON

Gene Symbol:RET
Accession:NM_001406777
Location:INTRON

Gene Symbol:RET
Accession:NM_001406792
Location:INTRON

Gene Symbol:RET
Accession:NM_001406786
Location:INTRON

Gene Symbol:RET
Accession:NM_001406790
Location:INTRON

Gene Symbol:RET
Accession:NM_001406781
Location:INTRON

Gene Symbol:RET
Accession:NM_001406770
Location:INTRON

Variant Samples
Additional References at PubMed
PMID:9536098   PMID:17576681   PMID:28492532  


Additional Information

Database Acc Id Source(s)
ClinVar RCV000824643 CLINVAR
dbSNP (RS) rs1588873485 CLINVAR
MedGen C4048306 CLINVAR
NCBI Gene RET CLINVAR
OMIM 164761 CLINVAR
SNOMED CT 61808009 CLINVAR