RGD:150467539 Rat Genome Database

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Variant: RGD:150467539 -  Homo sapiens

RGD ID: 150467539
RS ID: rs3027643
ClinVar ID: CV1269248
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: BTK  
Reference Nucleotide: C
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 X 100,611,432
GRCh38 X 101,356,444
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_001287345.2:c.1039-1750C>T
NM_000061.3:c.1350-176C>T
NM_001287344.2:c.1452-176C>T
LRG_128:g.34781C>T
More... 		07/09/2018 intron variant benign none provided

Variant Details
Variant Transcripts
Gene Symbol:BTK
Accession:NM_000061
Location:INTRON

Gene Symbol:BTK
Accession:NM_001287344
Location:INTRON

Gene Symbol:BTK
Accession:NM_001287345
Location:INTRON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV001694656 CLINVAR
dbSNP (RS) rs3027643 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene BTK CLINVAR
OMIM 300300 CLINVAR