Variant #0000929156 (NC_000006.11:g.144262694_144262696dup, NM_001080951.1:c.1266_1268dup (PLAGL1))

Chromosome 6
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.144262694_144262696dup
DNA change (hg38) -
Published as PLAGL1(NM_001080951.3):c.1266_1268dupGCA (p.Q423dup)
ISCN -
DB-ID PLAGL1_000009
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_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2023-07-07 10:10:56 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ZC2HC1B NM_001013623.2 ?/. - c.*3430_*3432dup r.(=) p.(=)
PLAGL1 NM_001080951.1 ?/. - c.1266_1268dup r.(?) p.(Gln423dup)


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