Genomic variant #0000366968

Individual ID 00163057
Chromosome 6
Allele Both (homozygous)
Affects function (as reported) Affects function
Affects function (by curator) Affects function
DNA change (genomic) (Relative to hg19 / GRCh37) g.76527300dup
DNA change (hg38) -
Published as 36-37insT
ISCN -
DB-ID MYO6_000002 See all 6 reported entries
Variant remarks homozygous
Reference PubMed: Ahmed et al., 2003
ClinVar ID -
dbSNP ID -
Origin Germline
Segregation -
Frequency 0/200 controls
Re-site -
VIP 0
Methylation -
Average frequency (large NGS studies) Variant not found in online data sets
Owner Anne-Françoise Roux
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

ClassClinical     

RNA change     

Protein     

P-domain     
MYO6 NM_004999.3 +/+ 2 c.36dup pathogenic r.(?) p.(Thr13Tyrfs*20) -



Screenings


AscendingScreening ID     

Template     

Technique     

Tissue     

Remarks     

Genes screened     

Variants found     

Owner     
0000163922 DNA SEQ - - MYO6 1 Anne-Françoise Roux