rs79549169 Rat Genome Database

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Variant: rs79549169 -  Homo sapiens

RGD ID: 15142446
RS ID: rs79549169
ClinVar ID: CV780118
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: CHD6  
Reference Nucleotide: A
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 20 40,141,481
GRCh38 20 41,512,842
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_032221.5:c.852+4T>C
NG_050686.1:g.110653T>C
NC_000020.11:g.41512842A>G
NC_000020.10:g.40141481A>G
More... 		12/31/2019 intron variant benign none provided

Variant Details
Variant Transcripts
Gene Symbol:CHD6
Accession:XM_011529080
Location:INTRON

Gene Symbol:CHD6
Accession:NM_032221
Location:INTRON

Gene Symbol:CHD6
Accession:XM_005260576
Location:INTRON

Gene Symbol:CHD6
Accession:XM_017028104
Location:INTRON

Gene Symbol:CHD6
Accession:XM_047440551
Location:INTRON

Gene Symbol:CHD6
Accession:XM_047440547
Location:INTRON

Gene Symbol:CHD6
Accession:XM_047440549
Location:INTRON

Gene Symbol:CHD6
Accession:XM_017028101
Location:INTRON

Gene Symbol:CHD6
Accession:XM_017028099
Location:INTRON

Gene Symbol:CHD6
Accession:XM_017028102
Location:INTRON

Gene Symbol:CHD6
Accession:XM_047440548
Location:INTRON

Gene Symbol:CHD6
Accession:XM_047440550
Location:INTRON

Gene Symbol:CHD6
Accession:XM_047440545
Location:INTRON

Gene Symbol:CHD6
Accession:XM_011529082
Location:INTRON

Gene Symbol:CHD6
Accession:XM_017028100
Location:INTRON

Gene Symbol:CHD6
Accession:XM_047440546
Location:INTRON

Variant Samples
Additional References at PubMed
PMID:28492532  


Additional Information

Database Acc Id Source(s)
ClinVar RCV000966491 CLINVAR
dbSNP (RS) rs79549169 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene CHD6 CLINVAR
OMIM 616114 CLINVAR