Variant #0000808778 (NC_000019.9:g.18979844G>T, NM_001492.4:c.681C>A (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.18979844G>T
DNA change (hg38) -
Published as GDF1(NM_001492.4):c.681C>A (p.(Cys227*)), GDF1(NM_001492.5):c.681C>A (p.C227*), GDF1(NM_001492.6):c.681C>A (p.C227*)
ISCN -
DB-ID GDF1_000002 See all 7 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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2021-09-17 14:40:49 +02:00 (CEST)
Date last edited 2023-04-16 21:50:28 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
GDF1 NM_001492.4 +/. - c.681C>A r.(?) p.(Cys227Ter)
UPF1 NM_002911.3 +/. - c.*2518G>T r.(=) p.(=)
CERS1 NM_021267.3 +/. - c.*950C>A r.(=) p.(=)


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