Variant #0000894887 (NC_000019.9:g.18979473_18979490dup, NM_001492.4:c.1036_1053dup (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.18979473_18979490dup
DNA change (hg38) -
Published as GDF1(NM_001492.6):c.1036_1053dupTCCGTGCTCTTCTTTGAC (p.S346_D351dup)
ISCN -
DB-ID GDF1_000058
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_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2022-11-01 13:41:49 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
GDF1 NM_001492.4 ?/. - c.1036_1053dup r.(?) p.(Ser346_Asp351dup)
UPF1 NM_002911.3 ?/. - c.*2147_*2164dup r.(=) p.(=)
CERS1 NM_021267.3 ?/. - c.*1305_*1322dup r.(=) p.(=)


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