RGD:10397280 Rat Genome Database

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Variant: RGD:10397280 -  Homo sapiens

RGD ID: 10397280
ClinVar ID: CV203842
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: ADSL  
Reference Nucleotide: T
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 22 40,750,242
GRCh38 22 40,354,238
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NG_007993.1:g.12739T>G
NC_000022.11:g.40354238T>G
NC_000022.10:g.40750242T>G
NM_000026.3:c.403-10T>G
More... 		07/24/2013 intron variant uncertain significance AllHighlyPenetrant

Variant Details
Variant Transcripts
Gene Symbol:ADSL
Accession:NM_000026
Location:INTRON

Gene Symbol:
Accession:
Location:INTRON

Gene Symbol:
Accession:
Location:INTRON

Gene Symbol:ADSL
Accession:NM_001410812
Location:INTRON

Gene Symbol:ADSL
Accession:XM_017028636
Location:INTRON

Gene Symbol:ADSL
Accession:NM_001363840
Location:INTRON

Gene Symbol:ADSL
Accession:XM_047441168
Location:INTRON

Gene Symbol:ADSL
Accession:NM_001410816
Location:INTRON

Gene Symbol:
Accession:
Location:INTRON

Gene Symbol:ADSL
Accession:NM_001317923
Location:INTRON

Gene Symbol:ADSL
Accession:NM_001410814
Location:INTRON

Gene Symbol:ADSL
Accession:NM_001123378
Location:INTRON

Gene Symbol:ADSL
Accession:NR_134256
Location:INTRON;NON-CODING

Variant Samples