RGD:28872107 Rat Genome Database

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Variant: RGD:28872107 -  Homo sapiens

RGD ID: 28872107
RS ID: rs1364938422
ClinVar ID: CV896555
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: CD2AP  
Reference Nucleotide: C
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 6 47,594,080
GRCh38 6 47,626,344
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NG_008878.1:g.153556C>G
NM_012120.3:c.*2117C>G
NM_012120.2:c.*2117C>G
NC_000006.12:g.47626344C>G
More... 		01/13/2018 3 prime utr variant uncertain significance
Disease Annotations     Click to see Annotation Detail View


Variant Details
Variant Transcripts
Gene Symbol:CD2AP
Accession:NM_012120
Location:3UTRS;EXON

Gene Symbol:CD2AP
Accession:XM_005248976
Location:3UTRS;EXON

Gene Symbol:CD2AP
Accession:XM_011514449
Location:3UTRS;EXON

Gene Symbol:CD2AP
Accession:XM_017010641
Location:INTRON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV001164252 CLINVAR
dbSNP (RS) rs1364938422 CLINVAR
MedGen C1842982 CLINVAR
NCBI Gene CD2AP CLINVAR
OMIM 604241 CLINVAR
  607832 CLINVAR