Screening #0000142191

Individual ID 00141351
Template DNA
Technique MAPH;PCRm
Tissue -
Remarks -
Variants found? 1
Owner name Ayfer Ulgenalp


Genes screened


AscendingSymbol     

Gene     

Chr     

Band

Transcripts     

Variants     

Unique variants     

Last updated     

Associated with diseases
DMD dystrophin X p21.2 1 18474 5617 2019-10-11 BMD, BMD/DMD, CMD-3B, DMD



Variants found

1 entry on 1 page. Showing entry 1.
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Chr     

Allele     

Effect     

AscendingDNA change (genomic) (hg19)     

DNA change (hg38)     

Published as     

ISCN     

DB-ID     

Variant remarks     

Reference     

ClinVar ID     

dbSNP ID     

Origin     

Segregation     

Frequency     

Re-site     

VIP     

Methylation     

Owner     

Gene     

Codon change     

IDbase Accession Number     

VariO/DNA     

VariO/Protein     

VariO/RNA     

Exon     

DNA change (cDNA)     

Haplotype     

ClassClinical     

RNA change     

Protein     

P-domain     

Exon_old     

DNA/Legacy     

Function/GVS     

Predict/AGVGD     

Predict/Grantham     

Predict/MutationTaster     

Predict/PolyPhen     

Predict/PolyPhenScore     

Predict/SIFT     

Predicted     

Type/DNA     

Conservation     

CpG     

Enzyme activity     

mRNA level     

Predict/CADD     

Predict/Splice     

Protein level     
X Unknown +/. g.(31986532_32235089)_(33229611_?)del g.(31968415_32216972)_(33211494_?)del c.-244_(6438+1_6439-1)del - DMD_010044 deletion incl. Dp427c - - - Germline - - - 0 - Ayfer Ulgenalp DMD - - - - - _0_44i NM_004006.2:c.-244_(6382_6538)del - pathogenic (recessive) r.0 p.0 - - - - - - - - - - - - - - - - - - -
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