ClinVar Miner

List of variants in gene DMD studied for See cases

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 46
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HGVS dbSNP gnomAD frequency
GRCh37/hg19 Xp21.1(chrX:31527227-31646780)x3
GRCh37/hg19 Xp21.1(chrX:31529262-31645888)x3
GRCh37/hg19 Xp21.1(chrX:31627576-31785116)x1
GRCh37/hg19 Xp21.1(chrX:31637969-31894898)x0
GRCh37/hg19 Xp21.1(chrX:31683623-31766614)x0
GRCh37/hg19 Xp21.1(chrX:31766614-31855217)x0
GRCh37/hg19 Xp21.1(chrX:31766614-31896429)x0
GRCh37/hg19 Xp21.1(chrX:31836968-31945018)x1
GRCh37/hg19 Xp21.1(chrX:31844447-31897253)x1
GRCh37/hg19 Xp21.1(chrX:31923771-32043955)x0
GRCh37/hg19 Xp21.1(chrX:31949273-32079092)x1
GRCh37/hg19 Xp21.1(chrX:31951570-32096169)x0
GRCh37/hg19 Xp21.1(chrX:31986184-31986956)x1
GRCh37/hg19 Xp21.1(chrX:32035638-32077563)x1
GRCh37/hg19 Xp21.1(chrX:32077637-32237871)x0
GRCh37/hg19 Xp21.1(chrX:32349168-32534563)x0
GRCh37/hg19 Xp21.1(chrX:32485353-32585911)x3
GRCh37/hg19 Xp21.1(chrX:32620055-33514149)x2
GRCh37/hg19 Xp21.1(chrX:32644702-32681484)x2
GRCh37/hg19 Xp21.1(chrX:33149703-33292999)x3
GRCh37/hg19 Xp21.1(chrX:33183494-33640512)x2
GRCh37/hg19 Xp21.1(chrX:33269852-34062091)x3
GRCh37/hg19 Xp21.2(chrX:31102254-31157224)x2
GRCh38/hg38 Xp21.1(chrX:31518752-31636035)x3
GRCh38/hg38 Xp21.1(chrX:31518960-31601824)x2
GRCh38/hg38 Xp21.1(chrX:31564763-31571376)x1
GRCh38/hg38 Xp21.1(chrX:31640772-31665565)x0
GRCh38/hg38 Xp21.1(chrX:31645986-31773985)x1
GRCh38/hg38 Xp21.1(chrX:31695292-31840818)x0
GRCh38/hg38 Xp21.1(chrX:31724913-31806626)x0
GRCh38/hg38 Xp21.1(chrX:31870708-31898871)x1
GRCh38/hg38 Xp21.1(chrX:31898812-32022323)x0
GRCh38/hg38 Xp21.1(chrX:32203741-32353533)x1
GRCh38/hg38 Xp21.1(chrX:32267823-32372572)x0
GRCh38/hg38 Xp21.1(chrX:32275729-32353585)x1
GRCh38/hg38 Xp21.1(chrX:32662366-32758964)x2
GRCh38/hg38 Xp21.1(chrX:32720062-32797373)x2
GRCh38/hg38 Xp21.1(chrX:32928883-33780762)x3
GRCh38/hg38 Xp21.1(chrX:33247944-33273382)x1
GRCh38/hg38 Xp21.2(chrX:31194383-31200627)x0
GRCh38/hg38 Xp21.2-21.1(chrX:31431098-31525874)x0
NM_004006.3(DMD):c.10141C>T (p.Arg3381Ter) rs104894790
NM_004006.3(DMD):c.3455T>A (p.Leu1152Ter)
NM_004006.3(DMD):c.3804G>C (p.Trp1268Cys) rs1569562573
NM_004006.3(DMD):c.7474_7477dup (p.Ile2493fs)
NM_004006.3(DMD):c.9808-2A>G rs1602456486

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