Variant #0000998951 (NC_000011.9:g.2181150G>A, NM_000207.2:c.265C>T (INS))

Chromosome 11
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.2181150G>A
DNA change (hg38) -
Published as INS(NM_001185098.2):c.265C>T (p.R89C)
ISCN -
DB-ID INS_000011 See all 4 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) Retrieve
Owner VKGL-NL_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2024-08-28 13:16:32 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

Haplotype     

RNA change     

Protein     
INS NM_000207.2 +/. - c.265C>T - r.(?) p.(Arg89Cys)
TH NM_000360.3 +/. - c.*4313C>T - r.(=) p.(=)
IGF2 NM_000612.4 +/. - c.-21698C>T - r.(?) p.(=)
INS-IGF2 NM_001042376.2 +/. - c.187+865C>T - r.(=) p.(=)
TH NM_199292.2 +/. - c.*4313C>T - r.(=) p.(=)


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