RGD:11611204 Rat Genome Database

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Variant: RGD:11611204 -  Homo sapiens

RGD ID: 11611204
RS ID: rs547875413
ClinVar ID: CV305781
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: CDCA7L  DNAH11  
Reference Nucleotide: T
Variant Nucleotide: C
Position
Assembly Chr Position
GRCh37 7 21,941,028
GRCh38 7 21,901,410
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NG_012886.2:g.363196T>C
NC_000007.14:g.21901410T>C
NC_000007.13:g.21941028T>C
NM_001127370.3:c.*912A>G
More... 		06/14/2016 3 prime utr variant uncertain significance
Disease Annotations     Click to see Annotation Detail View


Variant Details
Variant Transcripts
Gene Symbol:DNAH11
Accession:NM_001277115
Location:3UTRS;EXON

Gene Symbol:CDCA7L
Accession:NM_001127370
Location:3UTRS;EXON

Gene Symbol:CDCA7L
Accession:NM_018719
Location:3UTRS;EXON

Gene Symbol:CDCA7L
Accession:NM_001127371
Location:3UTRS;EXON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV000391956 CLINVAR
dbSNP (RS) rs547875413 CLINVAR
MedGen C0008780 CLINVAR
NCBI Gene CDCA7L CLINVAR
  DNAH11 CLINVAR
OMIM 603339 CLINVAR
  609685 CLINVAR