Variant #0000723792 (NC_000012.11:g.102811782C>G, NC_000012.11(NM_000618.3):c.402+1505G>C (IGF1))

Chromosome 12
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.102811782C>G
DNA change (hg38) -
Published as IGF1(NM_001111283.2):c.403-1G>C
ISCN -
DB-ID IGF1_000024
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) 0 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2021-02-08 18:36:18 +01:00 (CET)
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.402+1505G>C r.(=) p.(=)
IGF1 NM_001111283.1 +/. - c.403-1G>C r.spl? p.?


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