Variant #0000979513 (NC_000011.9:g.2185608C>T, NM_000207.2:c.-3228G>A (INS))

Chromosome 11
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.2185608C>T
DNA change (hg38) -
Published as TH(NM_000360.3):c.1349G>A (p.(Arg450His))
ISCN -
DB-ID IGF2_000102
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.-3228G>A - r.(?) p.(=)
TH NM_000360.3 ?/. - c.1349G>A - r.(?) p.(Arg450His)
IGF2 NM_000612.4 ?/. - c.-26156G>A - r.(?) p.(=)
INS-IGF2 NM_001042376.2 ?/. - c.-3228G>A - r.(?) p.(=)
TH NM_199292.2 ?/. - c.1442G>A - r.(?) p.(Arg481His)


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