Variant #0000977371 (NC_000006.11:g.76570745_76570746insTCCTAAAATGATTATTTCATTTTAG, NM_004999.3:c.1479_1480insTCCTAAAATGATTATTTCATTTTAG (MYO6))

Chromosome 6
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.76570745_76570746insTCCTAAAATGATTATTTCATTTTAG
DNA change (hg38) -
Published as -
ISCN -
DB-ID MYO6_000155
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner VKGL-NL_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2024-04-19 20:27:30 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

P-domain     
MYO6 NM_004999.3 +?/. - c.1479_1480insTCCTAAAATGATTATTTCATTTTAG r.(?) p.(Glu494Serfs*2) -


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