RGD:127289237 Rat Genome Database

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Variant: RGD:127289237 -  Homo sapiens

RGD ID: 127289237
RS ID: rs368796407
ClinVar ID: CV1130574
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: ATF6  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 1 161,928,232
GRCh38 1 161,958,442
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NG_029773.1:g.197199G>A
NC_000001.11:g.161958442G>A
NC_000001.10:g.161928232G>A
NM_007348.4:c.1805-4G>A
 01/01/2020 intron variant likely benign none provided

Variant Details
Variant Transcripts
Gene Symbol:ATF6
Accession:XM_011509309
Location:INTRON

Gene Symbol:ATF6
Accession:XM_047449542
Location:INTRON

Gene Symbol:ATF6
Accession:XM_011509308
Location:INTRON

Gene Symbol:ATF6
Accession:NM_007348
Location:INTRON

Gene Symbol:ATF6
Accession:XM_011509310
Location:INTRON

Gene Symbol:
Accession:
Location:INTRON

Gene Symbol:ATF6
Accession:NM_001410890
Location:INTRON

Variant Samples
Additional References at PubMed
PMID:28492532  


Additional Information

Database Acc Id Source(s)
ClinVar RCV001495565 CLINVAR
dbSNP (RS) rs368796407 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene ATF6 CLINVAR
OMIM 605537 CLINVAR