RGD:8622018 Rat Genome Database

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Variant: RGD:8622018 -  Homo sapiens

RGD ID: 8622018
RS ID: rs143051595
ClinVar ID: CV77034
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: KRT18  LOC106096416  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 12 53,344,232
GRCh38 12 52,950,448
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NG_008351.1:g.6578G>A
NC_000012.12:g.52950448G>A
NC_000012.11:g.53344232G>A
NM_000224.3:c.500+38G>A
More... 		2kb upstream variant|intron|intron variant not provided none provided

Variant Details
Variant Transcripts
Gene Symbol:KRT18
Accession:NM_199187
Location:INTRON

Gene Symbol:KRT18
Accession:NM_000224
Location:INTRON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV000056438 CLINVAR
dbSNP (RS) rs143051595 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene 106096416 CLINVAR
  KRT18 CLINVAR
OMIM 148070 CLINVAR