Variant #0000617483 (NC_000019.9:g.18980949C>T, NM_001492.4:c.168G>A (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.18980949C>T
DNA change (hg38) g.18870140C>T
Published as -
ISCN -
DB-ID GDF1_000047
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 2019-12-04 15:24:38 +01:00 (CET)
Date last edited 2020-07-15 16:24:08 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
GDF1 NM_001492.4 -?/. - c.168G>A r.(?) p.(Arg56=)
UPF1 NM_002911.3 -?/. - c.*3623C>T r.(=) p.(=)
CERS1 NM_021267.3 -?/. - c.*437G>A r.(=) p.(=)


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