RGD:150404394 Rat Genome Database

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Variant: RGD:150404394 -  Homo sapiens

RGD ID: 150404394
RS ID: rs13405107
ClinVar ID: CV1193146
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: ALK  
Reference Nucleotide: C
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 2 29,473,926
GRCh38 2 29,251,060
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NG_009445.1:g.675507G>A
NC_000002.12:g.29251060C>T
NM_004304.5:c.2204+45G>A
LRG_488:g.675507G>A
More... 		06/23/2018 intron variant likely benign none provided

Variant Details
Variant Transcripts
Gene Symbol:ALK
Accession:NM_004304
Location:INTRON

Gene Symbol:ALK
Accession:NM_001353765
Location:INTRON

Gene Symbol:ALK
Accession:XR_001738688
Location:INTRON;NON-CODING

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV001571120 CLINVAR
dbSNP (RS) rs13405107 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene ALK CLINVAR
OMIM 105590 CLINVAR