Variant #0000566689 (NC_000019.9:g.18981062G>C, NM_001492.4:c.55C>G (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.18981062G>C
DNA change (hg38) g.18870253G>C
Published as GDF1(NM_001492.6):c.55C>G (p.L19V)
ISCN -
DB-ID GDF1_000031 See all 2 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) 0.00029 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 2019-07-18 18:22:55 +02:00 (CEST)
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.55C>G r.(?) p.(Leu19Val)
UPF1 NM_002911.3 -?/. - c.*3736G>C r.(=) p.(=)
CERS1 NM_021267.3 -?/. - c.*324C>G r.(=) p.(=)


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