Variant #0000275096 (NC_000023.10:g.69672519G>C, DLG3(NM_021120.3):c.1145+643G>C)

Chromosome X
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.69672519G>C
DNA change (hg38) g.70452669G>C
Published as DLG3(NM_001166278.1):c.-2639G>C (p.(=)), DLG3(NM_020730.2):c.48G>C (p.L16F)
ISCN -
DB-ID DLG3_000041 See all 2 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) 0.00195 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
DLG3 NM_021120.3 -/. - c.1145+643G>C r.(=) p.(=)