RGD:15108416 Rat Genome Database

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Variant: RGD:15108416 -  Homo sapiens

RGD ID: 15108416
RS ID: rs377605184
ClinVar ID: CV776922
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: HDAC6  
Reference Nucleotide: G
Variant Nucleotide: C
Position
Assembly Chr Position
GRCh37 X 48,673,306
GRCh38 X 48,814,899
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_006044.3:c.1059+6G>C
NM_001321226.2:c.1059+6G>C
NM_001321227.2:c.1059+6G>C
NM_001321228.2:c.1059+6G>C
More... 		11/01/2022 intron variant likely benign none provided

Variant Details
Variant Transcripts
Gene Symbol:HDAC6
Accession:NM_001321229
Location:INTRON

Gene Symbol:HDAC6
Accession:XM_047441703
Location:INTRON

Gene Symbol:HDAC6
Accession:NM_001321226
Location:INTRON

Gene Symbol:HDAC6
Accession:XM_047441704
Location:INTRON

Gene Symbol:HDAC6
Accession:NM_001321227
Location:INTRON

Gene Symbol:HDAC6
Accession:XM_047441707
Location:INTRON

Gene Symbol:HDAC6
Accession:NM_001321230
Location:INTRON

Gene Symbol:HDAC6
Accession:NM_006044
Location:INTRON

Gene Symbol:HDAC6
Accession:NM_001321225
Location:INTRON

Gene Symbol:HDAC6
Accession:NM_001321228
Location:INTRON

Gene Symbol:HDAC6
Accession:NM_001321231
Location:INTRON

Gene Symbol:HDAC6
Accession:XM_047441705
Location:INTRON

Gene Symbol:HDAC6
Accession:XM_047441706
Location:INTRON

Gene Symbol:HDAC6
Accession:NR_135592
Location:INTRON;NON-CODING

Gene Symbol:HDAC6
Accession:NR_135593
Location:INTRON;NON-CODING

Gene Symbol:HDAC6
Accession:XR_007068179
Location:INTRON;NON-CODING

Gene Symbol:HDAC6
Accession:NR_135591
Location:INTRON;NON-CODING

Variant Samples
Additional References at PubMed
PMID:28492532  


Additional Information

Database Acc Id Source(s)
ClinVar RCV000938151 CLINVAR
dbSNP (RS) rs377605184 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene HDAC6 CLINVAR
OMIM 300272 CLINVAR