Variant #0000543469 (NC_000011.9:g.2186499C>T, INS(NM_000207.2):c.-4119G>A)

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.2186499C>T
DNA change (hg38) g.2165269C>T
Published as TH(NM_199292.3):c.1390G>A (p.V464M)
ISCN -
DB-ID IGF2_000054
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) 2.0E-5 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

Haplotype     

RNA change     

Protein     
INS NM_000207.2 ?/. - c.-4119G>A - r.(?) p.(=)
TH NM_000360.3 ?/. - c.1297G>A - r.(?) p.(Val433Met)
IGF2 NM_000612.4 ?/. - c.-27047G>A - r.(?) p.(=)
INS-IGF2 NM_001042376.2 ?/. - c.-4119G>A - r.(?) p.(=)
TH NM_199292.2 ?/. - c.1390G>A - r.(?) p.(Val464Met)