Variant #0000566664 (NC_000019.9:g.18976849T>G, NM_001492.4:c.*2557A>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.18976849T>G
DNA change (hg38) g.18866040T>G
Published as UPF1(NM_002911.3):c.3238-4T>G (p.?)
ISCN -
DB-ID GDF1_000012
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-07-15 16:13:57 +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.*2557A>C r.(=) p.(=)
UPF1 NM_002911.3 -?/. - c.3238-4T>G r.spl? p.?
CERS1 NM_021267.3 -?/. - c.*3945A>C r.(=) p.(=)


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