RGD:405280811 Rat Genome Database

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Variant: RGD:405280811 -  Homo sapiens

RGD ID: 405280811
ClinVar ID: CV3195742
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: NCOA1  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 2 24,975,030
GRCh38 2 24,752,161
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_001362950.1:c.3881+5G>A
NM_001362952.1:c.3881+5G>A
NM_001362954.1:c.3881+5G>A
NM_001362955.1:c.3881+5G>A
More... 		02/28/2024 intron variant uncertain significance NCOA1-related condition

Variant Details
Variant Transcripts
Gene Symbol:NCOA1
Accession:XM_047446155
Location:INTRON

Gene Symbol:NCOA1
Accession:NM_001362952
Location:INTRON

Gene Symbol:NCOA1
Accession:NM_147223
Location:INTRON

Gene Symbol:NCOA1
Accession:NM_003743
Location:INTRON

Gene Symbol:NCOA1
Accession:NM_001362954
Location:INTRON

Gene Symbol:NCOA1
Accession:XM_047446154
Location:INTRON

Gene Symbol:NCOA1
Accession:NM_001362950
Location:INTRON

Gene Symbol:NCOA1
Accession:XM_047446153
Location:INTRON

Gene Symbol:NCOA1
Accession:NM_147233
Location:INTRON

Gene Symbol:NCOA1
Accession:XM_047446151
Location:INTRON

Gene Symbol:NCOA1
Accession:XM_047446158
Location:INTRON

Gene Symbol:NCOA1
Accession:XM_047446157
Location:INTRON

Gene Symbol:NCOA1
Accession:NM_001362955
Location:INTRON

Gene Symbol:NCOA1
Accession:XM_047446152
Location:INTRON

Gene Symbol:NCOA1
Accession:XM_047446156
Location:INTRON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV003906973 CLINVAR
NCBI Gene NCOA1 CLINVAR
OMIM 602691 CLINVAR