RGD:150486203 Rat Genome Database

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Variant: RGD:150486203 -  Homo sapiens

RGD ID: 150486203
RS ID: rs10432556
ClinVar ID: CV1273962
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: ACVR1C  
Reference Nucleotide: G
Variant Nucleotide: C
Position
Assembly Chr Position
GRCh37 2 158,401,137
GRCh38 2 157,544,625
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_001111033.2:c.305-13A>G
NM_001111032.2:c.536-13A>G
NM_001111031.2:c.626-13A>G
NM_145259.3:c.776-13A>G
More... 		11/10/2018 intron variant benign none provided

Variant Details
Variant Transcripts
Gene Symbol:ACVR1C
Accession:NM_145259
Location:INTRON

Gene Symbol:ACVR1C
Accession:NM_001111033
Location:INTRON

Gene Symbol:ACVR1C
Accession:NM_001111032
Location:INTRON

Gene Symbol:ACVR1C
Accession:NM_001111031
Location:INTRON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV001698896 CLINVAR
dbSNP (RS) rs10432556 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene ACVR1C CLINVAR
OMIM 608981 CLINVAR