Variant #0001015773 (NC_000019.9:g.18979477_18979480del, NM_001492.4:c.1047_1050del (GDF1))

Chromosome 19
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.18979477_18979480del
DNA change (hg38) -
Published as GDF1(NM_001492.6):c.1047_1050del (p.(Phe349LeufsTer35)), GDF1(NM_001492.6):c.1047_1050delCTTT (p.F349Lfs*35)
ISCN -
DB-ID GDF1_000014 See all 5 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) 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 2024-10-29 21:08:56 +01:00 (CET)
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.1047_1050del r.(?) p.(Phe349LeufsTer35)
UPF1 NM_002911.3 +/. - c.*2151_*2154del r.(=) p.(=)
CERS1 NM_021267.3 +/. - c.*1316_*1319del r.(=) p.(=)


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.