Variant #0000543466 (NC_000011.9:g.2185575G>A, INS(NM_000207.2):c.-3195C>T)

Chromosome 11
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.2185575G>A
DNA change (hg38) g.2164345G>A
Published as -
ISCN -
DB-ID IGF2_000052 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_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

Haplotype     

RNA change     

Protein     
INS NM_000207.2 +?/. - c.-3195C>T - r.(?) p.(=)
TH NM_000360.3 +?/. - c.1382C>T - r.(?) p.(Pro461Leu)
IGF2 NM_000612.4 +?/. - c.-26123C>T - r.(?) p.(=)
INS-IGF2 NM_001042376.2 +?/. - c.-3195C>T - r.(?) p.(=)
TH NM_199292.2 +?/. - c.1475C>T - r.(?) p.(Pro492Leu)