RGD:150447820 Rat Genome Database

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Variant: RGD:150447820 -  Homo sapiens

RGD ID: 150447820
RS ID: rs13420239
ClinVar ID: CV1253459
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: ACVR1C  
Reference Nucleotide: A
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 2 158,412,878
GRCh38 2 157,556,366
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_145259.3:c.305-34T>C
NC_000002.11:g.158412878A>G
NM_001111032.2:c.305-5974T>C
NC_000002.12:g.157556366A>G
More... 		06/18/2021 intron variant benign none provided

Variant Details
Variant Transcripts
Gene Symbol:ACVR1C
Accession:NM_001111032
Location:INTRON

Gene Symbol:ACVR1C
Accession:NM_001111031
Location:INTRON

Gene Symbol:ACVR1C
Accession:NM_001111033
Location:INTRON

Gene Symbol:ACVR1C
Accession:NM_145259
Location:INTRON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV001667387 CLINVAR
dbSNP (RS) rs13420239 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene ACVR1C CLINVAR
OMIM 608981 CLINVAR