RGD:14729924 Rat Genome Database

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Variant: RGD:14729924 -  Homo sapiens

RGD ID: 14729924
RS ID: rs141235801
ClinVar ID: CV662597
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: LOC130000613  
Reference Nucleotide: C
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 8 74,888,253
GRCh38 8 73,976,018
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Clinical Significance Trait Synonyms
NM_017866.5:c.-264C>A
NC_000008.10:g.74888253C>A
NG_159362.1:g.6C>A
NC_000008.11:g.73976018C>A
More... 		06/14/2018 likely benign none provided

Variant Details
Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV000835441 CLINVAR
dbSNP (RS) rs141235801 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene LOC130000613 CLINVAR
  TMEM70 CLINVAR
OMIM 612418 CLINVAR