Variant #0000951260 (NC_000019.9:g.18980132G>T, NM_001492.4:c.393C>A (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.18980132G>T
DNA change (hg38) -
Published as GDF1(NM_001492.6):c.393C>A (p.F131L)
ISCN -
DB-ID GDF1_000061
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_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2023-11-27 17:35:39 +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.393C>A r.(?) p.(Phe131Leu)
UPF1 NM_002911.3 ?/. - c.*2806G>T r.(=) p.(=)
CERS1 NM_021267.3 ?/. - c.*662C>A r.(=) p.(=)


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