Variant #0000617479 (NC_000019.9:g.18980069_18980071dup, NM_001492.4:c.468_470dup (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.18980069_18980071dup
DNA change (hg38) g.18869260_18869262dup
Published as GDF1(NM_001492.4):c.470_471insGGC (p.(Ala158dup)), GDF1(NM_001492.5):c.468_470dupGGC (p.A158dup), GDF1(NM_001492.6):c.468_470dupGGC (p.A158dup)
ISCN -
DB-ID GDF1_000028 See all 5 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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2019-12-04 15:24:38 +01:00 (CET)
Date last edited 2021-09-17 14:40:49 +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.468_470dup r.(?) p.(Ala158dup)
UPF1 NM_002911.3 -?/. - c.*2743_*2745dup r.(=) p.(=)
CERS1 NM_021267.3 -?/. - c.*737_*739dup r.(=) p.(=)


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