rs267607664 Rat Genome Database

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Variant: rs267607664 -  Homo sapiens

RGD ID: 8622404
RS ID: rs267607664
ClinVar ID: CV77423
Genic Status: GENIC
Type: deletion (SO:0000159) 
Associated Genes: KRT8  
Reference Nucleotide: G
Variant Nucleotide: -
Position
Assembly Chr Position
GRCh37 12 53,292,235
GRCh38 12 52,898,451
JBrowse: View Region in Genome Browser (JBrowse)
Model



HGVS Name(s)
Last Evaluated
Molecular Consequence
Clinical Significance
Trait Synonyms
NM_002273.4:c.1261+11del
NM_002273.3:c.1261+10delC
NC_000012.11:g.53292236del
NM_001256293.2:c.1261+11del
More... 		intron variant not provided none provided

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Database
Acc Id
Source(s)
ClinVar RCV000056930 CLINVAR
dbSNP (RS) rs267607664 CLINVAR
MedGen CN517202 CLINVAR
NCBI Gene KRT8 CLINVAR
OMIM 148060 CLINVAR