Variant #0000862475 (NC_000011.9:g.2181243G>A, NC_000011.9(NM_000207.2):c.188-16C>T (INS))

Chromosome 11
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.2181243G>A
DNA change (hg38) -
Published as INS(NM_000207.2):c.188-16C>T (p.(=))
ISCN -
DB-ID IGF2_000077
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) 0.00125 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2022-05-09 15:51:19 +02:00 (CEST)
Date last edited 2022-11-01 13:01:21 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

Haplotype     

RNA change     

Protein     
INS NM_000207.2 -/. - c.188-16C>T - r.(=) p.(=)
TH NM_000360.3 -/. - c.*4220C>T - r.(=) p.(=)
IGF2 NM_000612.4 -/. - c.-21791C>T - r.(?) p.(=)
INS-IGF2 NM_001042376.2 -/. - c.187+772C>T - r.(=) p.(=)
TH NM_199292.2 -/. - c.*4220C>T - r.(=) p.(=)


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.