RGD:152047757 Rat Genome Database

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Variant: RGD:152047757 -  Homo sapiens

RGD ID: 152047757
RS ID: rs373631623
ClinVar ID: CV1580484
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: NEDD4L  
Reference Nucleotide: C
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 18 56,040,390
GRCh38 18 58,373,158
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_001144964.1:c.1894-16C>T
NM_001144966.3:c.1894-16C>T
NM_001243960.2:c.2065-16C>T
NM_001144969.2:c.2173-16C>T
More... 		07/27/2021 intron variant likely benign none provided

Variant Details
Variant Transcripts
Gene Symbol:NEDD4L
Accession:NM_001144967
Location:INTRON

Gene Symbol:NEDD4L
Accession:NM_015277
Location:INTRON

Gene Symbol:NEDD4L
Accession:NM_001144964
Location:INTRON

Gene Symbol:NEDD4L
Accession:NM_001144971
Location:INTRON

Gene Symbol:NEDD4L
Accession:NM_001144965
Location:INTRON

Gene Symbol:NEDD4L
Accession:NM_001144968
Location:INTRON

Gene Symbol:NEDD4L
Accession:NM_001144969
Location:INTRON

Gene Symbol:NEDD4L
Accession:NM_001144970
Location:INTRON

Gene Symbol:NEDD4L
Accession:NM_001144966
Location:INTRON

Gene Symbol:NEDD4L
Accession:NM_001243960
Location:INTRON

Gene Symbol:NEDD4L
Accession:XM_005266658
Location:INTRON

Gene Symbol:NEDD4L
Accession:XM_005266660
Location:INTRON

Gene Symbol:NEDD4L
Accession:XM_005266663
Location:INTRON

Gene Symbol:NEDD4L
Accession:XM_006722426
Location:INTRON

Gene Symbol:NEDD4L
Accession:XM_006722428
Location:INTRON

Gene Symbol:NEDD4L
Accession:XM_006722430
Location:INTRON

Gene Symbol:NEDD4L
Accession:XM_006722421
Location:INTRON

Gene Symbol:NEDD4L
Accession:XM_006722424
Location:INTRON

Gene Symbol:NEDD4L
Accession:XM_006722425
Location:INTRON

Gene Symbol:NEDD4L
Accession:XM_011525887
Location:INTRON

Gene Symbol:NEDD4L
Accession:XM_017025678
Location:INTRON

Gene Symbol:NEDD4L
Accession:XM_017025679
Location:INTRON

Gene Symbol:NEDD4L
Accession:XM_017025681
Location:INTRON

Gene Symbol:NEDD4L
Accession:XM_017025676
Location:INTRON

Gene Symbol:NEDD4L
Accession:XM_017025677
Location:INTRON

Gene Symbol:NEDD4L
Accession:XM_024451136
Location:INTRON

Gene Symbol:NEDD4L
Accession:XM_024451135
Location:INTRON

Gene Symbol:NEDD4L
Accession:XM_024451129
Location:INTRON

Gene Symbol:NEDD4L
Accession:XM_024451131
Location:INTRON

Gene Symbol:NEDD4L
Accession:XM_024451134
Location:INTRON

Gene Symbol:NEDD4L
Accession:XM_047437406
Location:INTRON

Gene Symbol:NEDD4L
Accession:XM_047437407
Location:INTRON

Gene Symbol:NEDD4L
Accession:XM_047437408
Location:INTRON

Gene Symbol:NEDD4L
Accession:XM_047437421
Location:INTRON

Gene Symbol:NEDD4L
Accession:XM_047437418
Location:INTRON

Gene Symbol:NEDD4L
Accession:XM_047437420
Location:INTRON

Gene Symbol:NEDD4L
Accession:XM_047437419
Location:INTRON

Gene Symbol:NEDD4L
Accession:XM_047437417
Location:INTRON

Gene Symbol:NEDD4L
Accession:XM_047437402
Location:INTRON

Gene Symbol:NEDD4L
Accession:XM_047437404
Location:INTRON

Gene Symbol:NEDD4L
Accession:XM_047437409
Location:INTRON

Gene Symbol:NEDD4L
Accession:XM_047437410
Location:INTRON

Gene Symbol:NEDD4L
Accession:XM_047437403
Location:INTRON

Gene Symbol:NEDD4L
Accession:XM_047437405
Location:INTRON

Gene Symbol:NEDD4L
Accession:XM_047437414
Location:INTRON

Gene Symbol:NEDD4L
Accession:XM_047437411
Location:INTRON

Gene Symbol:NEDD4L
Accession:XM_047437413
Location:INTRON

Gene Symbol:NEDD4L
Accession:XM_047437412
Location:INTRON

Gene Symbol:NEDD4L
Accession:XM_047437415
Location:INTRON

Gene Symbol:NEDD4L
Accession:XM_047437416
Location:INTRON

Variant Samples
Additional References at PubMed
PMID:28492532  


Additional Information

Database Acc Id Source(s)
ClinVar RCV002166471 CLINVAR
dbSNP (RS) rs373631623 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene NEDD4L CLINVAR
OMIM 606384 CLINVAR