Variant #0000566668 (NC_000019.9:g.18979634C>G, NM_001492.4:c.891G>C (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.18979634C>G
DNA change (hg38) g.18868825C>G
Published as GDF1(NM_001492.5):c.891G>C (p.Q297H), GDF1(NM_001492.6):c.891G>C (p.(Gln297His))
ISCN -
DB-ID GDF1_000016 See all 3 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_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 2025-05-05 21:14:00 +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.891G>C r.(?) p.(Gln297His)
UPF1 NM_002911.3 ?/. - c.*2308C>G r.(=) p.(=)
CERS1 NM_021267.3 ?/. - c.*1160G>C r.(=) p.(=)


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