Variant #0000566676 (NC_000019.9:g.18979924C>G, NM_001492.4:c.601G>C (GDF1))

Chromosome 19
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.18979924C>G
DNA change (hg38) g.18869115C>G
Published as -
ISCN -
DB-ID GDF1_000022
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_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
GDF1 NM_001492.4 -?/. - c.601G>C r.(?) p.(Ala201Pro)
UPF1 NM_002911.3 -?/. - c.*2598C>G r.(=) p.(=)
CERS1 NM_021267.3 -?/. - c.*870G>C r.(=) p.(=)


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