RGD:150419836 Rat Genome Database

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Variant: RGD:150419836 -  Homo sapiens

RGD ID: 150419836
RS ID: rs187395120
ClinVar ID: CV1197810
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: MCPH1-DT  
Reference Nucleotide: T
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 8 6,264,038
GRCh38 8 6,406,517
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NG_016619.2:g.4926T>G
NC_000008.11:g.6406517T>G
NC_000008.10:g.6264038T>G
NR_040040.1:n.32A>C
 08/24/2019 non-coding transcript variant likely benign none provided

Variant Details
Variant Transcripts
Gene Symbol:MCPH1-DT
Accession:NR_040040
Location:EXON;NON-CODING

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV001577353 CLINVAR
dbSNP (RS) rs187395120 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene MCPH1 CLINVAR
  MCPH1-DT CLINVAR
OMIM 607117 CLINVAR