Variant #0000334540 (NC_000023.10:g.69669205G>T, DLG3(NM_021120.3):c.409-4G>T)

Chromosome X
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.69669205G>T
DNA change (hg38) g.70449355G>T
Published as DLG3(NM_020730.2):c.-3267G>T (p.(=)), DLG3(NM_021120.3):c.409-4G>T, DLG3(NM_021120.4):c.409-4G>T
ISCN -
DB-ID DLG3_000039 See all 3 reported entries
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) 0.00102 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2021-09-17 14:40:49 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
DLG3 NM_021120.3 ?/. - c.409-4G>T r.spl? p.?