Variant #0000979516 (NC_000011.9:g.2186488G>A, NM_000207.2:c.-4108C>T (INS))

Chromosome 11
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.2186488G>A
DNA change (hg38) -
Published as INS(NM_000207.2):c.-4108C>T (p.(=))
ISCN -
DB-ID IGF2_000105
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 2024-04-19 20:27:30 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

Haplotype     

RNA change     

Protein     
INS NM_000207.2 -?/. - c.-4108C>T - r.(?) p.(=)
TH NM_000360.3 -?/. - c.1308C>T - r.(?) p.(=)
IGF2 NM_000612.4 -?/. - c.-27036C>T - r.(?) p.(=)
INS-IGF2 NM_001042376.2 -?/. - c.-4108C>T - r.(?) p.(=)
TH NM_199292.2 -?/. - c.1401C>T - r.(?) p.(=)


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