Variant #0000985303 (NC_000023.10:g.69672543G>T, NC_000023.10(NM_021120.3):c.1145+667G>T (DLG3))

Chromosome X
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.69672543G>T
DNA change (hg38) -
Published as -
ISCN -
DB-ID DLG3_000084
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs757449904
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner MobiDetails
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by MobiDetails
Date created 2024-05-16 14:19:01 +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     
DLG3 NM_021120.3 -?/. - c.1145+667G>T r.(?) p.(?)


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