Variant #0001046338 (NC_000012.11:g.102796352_102796355del, NC_000012.11(NM_000618.3):c.403-6_403-3del (IGF1))

Chromosome 12
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.102796352_102796355del
DNA change (hg38) -
Published as IGF1(NM_000618.3):c.403-6_403-3del (p.?)
ISCN -
DB-ID IGF1_000042
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2025-07-08 13:22:38 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
IGF1 NM_000618.3 ?/. - c.403-6_403-3del r.spl? p.?
IGF1 NM_001111283.1 ?/. - c.452-6_452-3del r.spl? p.?


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