Variant #0000905190 (NC_000012.11:g.102813396C>T, IGF1(NM_000618.3):c.293G>A)

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.102813396C>T
DNA change (hg38) -
Published as -
ISCN -
DB-ID IGF1_000037 See all 2 reported entries
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs1316717107
Origin Unknown
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 1.0E-5 View details
Owner MobiDetails
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by MobiDetails
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
IGF1 NM_000618.3 ?/. - c.293G>A r.(?) p.(Arg98Gln)