RGD:150507170 Rat Genome Database

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Variant: RGD:150507170 -  Homo sapiens

RGD ID: 150507170
RS ID: rs153924
ClinVar ID: CV1211109
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: ANKH  
Reference Nucleotide: A
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 5 14,755,771
GRCh38 5 14,755,662
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
LRG_1362t1:c.516+199T>G
NM_054027.6:c.516+199T>G
LRG_1362:g.121124T>G
NG_008273.2:g.121124T>G
More... 		11/10/2018 intron variant benign none provided

Variant Details
Variant Transcripts
Gene Symbol:ANKH
Accession:NM_054027
Location:INTRON

Gene Symbol:ANKH
Accession:XM_011514067
Location:INTRON

Gene Symbol:ANKH
Accession:XM_017009644
Location:INTRON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV001596227 CLINVAR
dbSNP (RS) rs153924 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene ANKH CLINVAR
OMIM 605145 CLINVAR