RGD:14706137 Rat Genome Database

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Variant: RGD:14706137 -  Homo sapiens

RGD ID: 14706137
RS ID: rs1639119
ClinVar ID: CV671188
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: ANOS1  
Reference Nucleotide: C
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 X 8,508,062
GRCh38 X 8,540,021
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NC_000023.10:g.8508062C>T
NM_000216.2:c.1355-263G>A
NM_000216.4:c.1355-263G>A
NG_007088.2:g.197166G>A
More... 		06/19/2018 intron variant benign none provided

Variant Details
Variant Transcripts
Gene Symbol:ANOS1
Accession:NM_000216
Location:INTRON

Gene Symbol:ANOS1
Accession:XM_005274501
Location:INTRON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV000826427 CLINVAR
dbSNP (RS) rs1639119 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene ANOS1 CLINVAR
OMIM 300836 CLINVAR