Variant #0000546230 (NC_000012.11:g.102869434C>T, IGF1(NM_000618.3):c.207G>A)

Chromosome 12
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.102869434C>T
DNA change (hg38) g.102475656C>T
Published as IGF1(NM_000618.3):c.207G>A (p.(Arg69=)), IGF1(NM_001111283.3):c.207G>A (p.R69=)
ISCN -
DB-ID IGF1_000011 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) 0.00146 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
IGF1 NM_000618.3 -?/. - c.207G>A r.(?) p.(Arg69=)
IGF1 NM_001111283.1 -?/. - c.207G>A r.(?) p.(Arg69=)