RGD:150543503 Rat Genome Database

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Variant: RGD:150543503 -  Homo sapiens

RGD ID: 150543503
ClinVar ID: CV1309492
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: ERCC3  
Reference Nucleotide: C
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 2 128,046,908
GRCh38 2 127,289,332
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_001303418.1:c.630+5G>A
NC_000002.11:g.128046908C>T
NC_000002.12:g.127289332C>T
NM_001303418.2:c.630+5G>A
More... 		11/03/2021 intron variant uncertain significance none provided

Variant Details
Variant Transcripts
Gene Symbol:ERCC3
Accession:XM_011510794
Location:INTRON

Gene Symbol:ERCC3
Accession:NM_001303418
Location:INTRON

Gene Symbol:ERCC3
Accession:NM_000122
Location:INTRON

Gene Symbol:ERCC3
Accession:XM_011510795
Location:INTRON

Gene Symbol:ERCC3
Accession:NM_001303416
Location:INTRON

Variant Samples