Variant #0000566672 (NC_000019.9:g.18979795G>C, NM_001492.4:c.730C>G (GDF1))

Chromosome 19
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.18979795G>C
DNA change (hg38) g.18868986G>C
Published as GDF1(NM_001492.5):c.730C>G (p.L244V)
ISCN -
DB-ID GDF1_000020
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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
GDF1 NM_001492.4 ?/. - c.730C>G r.(?) p.(Leu244Val)
UPF1 NM_002911.3 ?/. - c.*2469G>C r.(=) p.(=)
CERS1 NM_021267.3 ?/. - c.*999C>G r.(=) p.(=)


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.