Variant #0000543455 (NC_000011.9:g.2182104G>C, NM_000207.2:c.98C>G (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.2182104G>C
DNA change (hg38) g.2160874G>C
Published as INS(NM_000207.2):c.98C>G (p.(Ser33*))
ISCN -
DB-ID IGF2_000043
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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2022-11-01 13:01:21 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

Haplotype     

RNA change     

Protein     
INS NM_000207.2 +/. - c.98C>G - r.(?) p.(Ser33Ter)
TH NM_000360.3 +/. - c.*3359C>G - r.(=) p.(=)
IGF2 NM_000612.4 +/. - c.-22652C>G - r.(?) p.(=)
INS-IGF2 NM_001042376.2 +/. - c.98C>G - r.(?) p.(Ser33Ter)
TH NM_199292.2 +/. - c.*3359C>G - r.(=) p.(=)


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