RGD:15101280 Rat Genome Database

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Variant: RGD:15101280 -  Homo sapiens

RGD ID: 15101280
RS ID: rs141660196
ClinVar ID: CV731442
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: H2BW1  
Reference Nucleotide: A
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 X 103,267,327
GRCh38 X 104,012,755
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_001002916.4:c.492-7T>C
NM_001002916.5:c.408-7T>C
NG_016406.2:g.5934T>C
NC_000023.11:g.104012755A>G
More... 		12/31/2019 intron variant benign none provided

Variant Details
Variant Transcripts
Gene Symbol:H2BW1
Accession:NM_001002916
Location:INTRON

Variant Samples
Additional References at PubMed
PMID:28492532  


Additional Information

Database Acc Id Source(s)
ClinVar RCV000892256 CLINVAR
dbSNP (RS) rs141660196 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene H2BW1 CLINVAR
OMIM 300507 CLINVAR