Variant #0001046687 (NC_000018.9:g.19057249_19057250insT, NM_001142966.1:c.2488_2489insT (GREB1L))

Chromosome 18
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.19057249_19057250insT
DNA change (hg38) -
Published as GREB1L(NM_001142966.2):c.2488_2489insT (p.T830Ifs*10)
ISCN -
DB-ID GREB1L_000092
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_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2025-07-08 13:22:38 +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     
GREB1L NM_001142966.1 +/. - c.2488_2489insT r.(?) p.(Thr830Ilefs*10)


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