RGD:15106738 Rat Genome Database

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Variant: RGD:15106738 -  Homo sapiens

RGD ID: 15106738
RS ID: rs1602035340
ClinVar ID: CV773975
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: DMD  
Reference Nucleotide: A
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 X 31,152,310
GRCh38 X 31,134,193
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_004013.3:c.3543T>C
NM_004017.3:c.1680T>C
NM_004018.3:c.1680T>C
NM_004015.3:c.1719T>C
More... 		05/20/2018 synonymous variant likely benign Muscular dystrophy, pseudohypertrophic progressive, Duchenne type
Disease Annotations     Click to see Annotation Detail View


Variant Details
Variant Transcripts
Gene Symbol:DMD
Accession:XM_006724469
Location:EXON

Gene Symbol:DMD
Accession:NM_004023
Location:EXON

Gene Symbol:DMD
Accession:NM_004020
Location:EXON

Gene Symbol:DMD
Accession:XM_006724468
Location:EXON

Gene Symbol:DMD
Accession:XM_011545467
Location:EXON

Gene Symbol:DMD
Accession:XM_006724473
Location:EXON

Gene Symbol:DMD
Accession:NM_004021
Location:EXON

Gene Symbol:DMD
Accession:NM_004010
Location:EXON

Gene Symbol:DMD
Accession:NM_004017
Location:EXON

Gene Symbol:DMD
Accession:XM_006724475
Location:EXON

Gene Symbol:DMD
Accession:NM_004014
Location:EXON

Gene Symbol:DMD
Accession:NM_004015
Location:EXON

Gene Symbol:DMD
Accession:NM_004012
Location:EXON

Gene Symbol:DMD
Accession:NM_004011
Location:EXON

Gene Symbol:DMD
Accession:NM_004022
Location:EXON

Gene Symbol:DMD
Accession:NM_004006
Location:EXON

Gene Symbol:DMD
Accession:NM_004013
Location:EXON

Gene Symbol:DMD
Accession:NM_004018
Location:EXON

Gene Symbol:DMD
Accession:NM_000109
Location:EXON

Gene Symbol:DMD
Accession:NM_004016
Location:EXON

Gene Symbol:DMD
Accession:XM_006724470
Location:EXON

Gene Symbol:DMD
Accession:NM_004009
Location:EXON

Gene Symbol:DMD
Accession:XM_006724474
Location:EXON

Gene Symbol:DMD
Accession:XM_017029328
Location:EXON

Gene Symbol:DMD
Accession:NM_004019
Location:INTRON

Gene Symbol:DMD
Accession:XM_011545468
Location:INTRON

Gene Symbol:DMD
Accession:XM_017029330
Location:INTRON

Gene Symbol:DMD
Accession:XM_017029329
Location:INTRON

Gene Symbol:DMD
Accession:XM_047441889
Location:INTRON

Gene Symbol:DMD
Accession:XM_011545469
Location:INTRON

Variant Samples
Additional References at PubMed
PMID:28492532  


Additional Information

Database Acc Id Source(s)
ClinVar RCV001431462 CLINVAR
dbSNP (RS) rs1602035340 CLINVAR
MedGen C0013264 CLINVAR
NCBI Gene DMD CLINVAR
OMIM 300377 CLINVAR
  310200 CLINVAR
SNOMED CT 76670001 CLINVAR