rs1566906885 Rat Genome Database

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Variant: rs1566906885 -  Homo sapiens

RGD ID: 13831779
RS ID: rs1566906885
ClinVar ID: CV582276
Genic Status: GENIC
Type: insertion (SO:0000667) 
Associated Genes: FAN1  
Reference Nucleotide: -
Variant Nucleotide: AGTGCAT
Position
Assembly Chr Position
GRCh37 15 31,197,537
GRCh38 15 30,905,334
JBrowse: View Region in Genome Browser (JBrowse)
Model



HGVS Name(s)
Last Evaluated
Molecular Consequence
Clinical Significance
Trait Synonyms
NP_055782.3:p.Pro227fs
NM_014967.5:c.671_677dup
NG_032946.2:g.6483_6489dup
NC_000015.10:g.30905334_30905340dup
More... 		09/16/2018 frameshift variant uncertain significance none provided

.
PMID:25741868  



Database
Acc Id
Source(s)
ClinVar RCV000722461 CLINVAR
dbSNP (RS) rs1566906885 CLINVAR
MedGen CN517202 CLINVAR
NCBI Gene FAN1 CLINVAR
OMIM 613534 CLINVAR