Variant #0001027203 (NC_000019.9:g.18979434A>G, NM_001492.4:c.1091T>C (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.18979434A>G
DNA change (hg38) -
Published as -
ISCN -
DB-ID GDF1_000068
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) 0.00051 View details
Owner VKGL-NL_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2025-02-07 18:57:27 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
GDF1 NM_001492.4 +/. - c.1091T>C r.(?) p.(Met364Thr)
UPF1 NM_002911.3 +/. - c.*2108A>G r.(=) p.(=)
CERS1 NM_021267.3 +/. - c.*1360T>C r.(=) p.(=)


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