Variant #0000270818 (NC_000010.10:g.79588623_79588629del, DLG5(NM_004747.3):c.2289+13_2289+19del)

Chromosome 10
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.79588623_79588629del
DNA change (hg38) g.77828865_77828871del
Published as DLG5(NM_004747.4):c.2289+13_2289+19delGCTGGAG
ISCN -
DB-ID DLG5_000004
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP 0
Methylation -
Average frequency (gnomAD v.2.1.1) Variant not found in online data sets
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
DLG5 NM_004747.3 -?/. - c.2289+13_2289+19del r.(=) p.(=)