Variant #0000543477 (NC_000011.9:g.2187234T>A, NM_000207.2:c.-4854A>T (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.2187234T>A
DNA change (hg38) g.2166004T>A
Published as TH(NM_000360.3):c.1102A>T (p.(Thr368Ser)), TH(NM_199292.2):c.1195A>T (p.T399S)
ISCN -
DB-ID IGF2_000061 See all 2 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_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 2024-02-26 20:06:56 +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.-4854A>T - r.(?) p.(=)
TH NM_000360.3 ?/. - c.1102A>T - r.(?) p.(Thr368Ser)
IGF2 NM_000612.4 ?/. - c.-27782A>T - r.(?) p.(=)
INS-IGF2 NM_001042376.2 ?/. - c.-4854A>T - r.(?) p.(=)
TH NM_199292.2 ?/. - c.1195A>T - r.(?) p.(Thr399Ser)


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