RGD:150434918 Rat Genome Database

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Variant: RGD:150434918 -  Homo sapiens

RGD ID: 150434918
RS ID: rs76187272
ClinVar ID: CV1216010
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: ACVR1C  
Reference Nucleotide: C
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 2 158,390,626
GRCh38 2 157,534,114
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_001111032.2:c.1117-71G>A
NM_001111031.2:c.1207-71G>A
NM_145259.3:c.1357-71G>A
NM_001111033.2:c.886-71G>A
More... 		06/18/2021 intron variant benign none provided

Variant Details
Variant Transcripts
Gene Symbol:ACVR1C
Accession:NM_001111031
Location:INTRON

Gene Symbol:ACVR1C
Accession:NM_145259
Location:INTRON

Gene Symbol:ACVR1C
Accession:NM_001111033
Location:INTRON

Gene Symbol:ACVR1C
Accession:NM_001111032
Location:INTRON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV001609200 CLINVAR
dbSNP (RS) rs76187272 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene ACVR1C CLINVAR
OMIM 608981 CLINVAR