Variant #0000982793 (NC_000017.10:g.73612491_73612496dup, NM_004259.6:c.*11035_*11040dup (RECQL5))

Chromosome 17
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.73612491_73612496dup
DNA change (hg38) -
Published as MYO15B(NM_001309242.1):c.6094_6099dup (p.(Glu2032_Glu2033dup))
ISCN -
DB-ID RECQL5_000081
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
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     
RECQL5 NM_004259.6 -?/. - c.*11035_*11040dup r.(=) p.(=)


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