RGD:150543196 Rat Genome Database

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Variant: RGD:150543196 -  Homo sapiens

RGD ID: 150543196
RS ID: rs375695147
ClinVar ID: CV1309357
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: ERBB2  
Reference Nucleotide: C
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 17 37,866,588
GRCh38 17 39,710,335
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_001382802.1:c.643+454C>T
NM_001005862.3:c.670-5C>T
NM_001289938.2:c.670-5C>T
NM_001382782.1:c.670-5C>T
More... 		11/03/2021 intron variant uncertain significance none provided

Variant Details
Variant Transcripts
Gene Symbol:ERBB2
Accession:NM_001382782
Location:INTRON

Gene Symbol:ERBB2
Accession:NM_001382783
Location:INTRON

Gene Symbol:ERBB2
Accession:NM_001382786
Location:INTRON

Gene Symbol:ERBB2
Accession:NM_001382785
Location:INTRON

Gene Symbol:ERBB2
Accession:NM_001382796
Location:INTRON

Gene Symbol:ERBB2
Accession:NM_001382805
Location:INTRON

Gene Symbol:ERBB2
Accession:NM_001382793
Location:INTRON

Gene Symbol:ERBB2
Accession:NM_001382804
Location:INTRON

Gene Symbol:ERBB2
Accession:NM_001382790
Location:INTRON

Gene Symbol:ERBB2
Accession:NM_001289936
Location:INTRON

Gene Symbol:ERBB2
Accession:NM_001005862
Location:INTRON

Gene Symbol:ERBB2
Accession:NM_001382797
Location:INTRON

Gene Symbol:ERBB2
Accession:NM_001382787
Location:INTRON

Gene Symbol:ERBB2
Accession:NM_001382800
Location:INTRON

Gene Symbol:ERBB2
Accession:NM_001382791
Location:INTRON

Gene Symbol:ERBB2
Accession:NM_001382784
Location:INTRON

Gene Symbol:ERBB2
Accession:NM_001382789
Location:INTRON

Gene Symbol:ERBB2
Accession:NM_001382803
Location:INTRON

Gene Symbol:ERBB2
Accession:NM_001382794
Location:INTRON

Gene Symbol:ERBB2
Accession:NM_001382802
Location:INTRON

Gene Symbol:ERBB2
Accession:NM_001289938
Location:INTRON

Gene Symbol:ERBB2
Accession:NM_001289937
Location:INTRON

Gene Symbol:ERBB2
Accession:NM_001382795
Location:INTRON

Gene Symbol:ERBB2
Accession:NM_001382801
Location:INTRON

Gene Symbol:ERBB2
Accession:XM_047435590
Location:INTRON

Gene Symbol:ERBB2
Accession:NM_001382806
Location:INTRON

Gene Symbol:ERBB2
Accession:NM_001382799
Location:INTRON

Gene Symbol:ERBB2
Accession:NM_004448
Location:INTRON

Gene Symbol:ERBB2
Accession:NM_001382798
Location:INTRON

Gene Symbol:ERBB2
Accession:NM_001382788
Location:INTRON

Gene Symbol:ERBB2
Accession:NM_001382792
Location:INTRON

Gene Symbol:ERBB2
Accession:NR_110535
Location:INTRON;NON-CODING

Variant Samples
Additional References at PubMed
PMID:25741868  


Additional Information

Database Acc Id Source(s)
ClinVar RCV003238429 CLINVAR
dbSNP (RS) rs375695147 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene ERBB2 CLINVAR
OMIM 164870 CLINVAR