Variant #0001042807 (NC_000019.9:g.18980907dup, NM_001492.4:c.214dup (GDF1))

Chromosome 19
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.18980907dup
DNA change (hg38) -
Published as GDF1(NM_001492.6):c.214dup (p.(Gln72Profs*55))
ISCN -
DB-ID GDF1_000070
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2025-05-05 21:14:00 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
GDF1 NM_001492.4 ?/. - c.214dup r.(?) p.(Gln72Profs*55)
UPF1 NM_002911.3 ?/. - c.*3581dup r.(?) p.(=)
CERS1 NM_021267.3 ?/. - c.*483dup r.(?) p.(=)


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