Variant #0000543472 (NC_000011.9:g.2186541C>T, INS(NM_000207.2):c.-4161G>A)

Chromosome 11
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.2186541C>T
DNA change (hg38) g.2165311C>T
Published as TH(NM_000360.3):c.1255G>A (p.(Val419Met)), TH(NM_199292.3):c.1348G>A (p.V450M)
ISCN -
DB-ID TH_000008 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) 0.00045 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

Haplotype     

RNA change     

Protein     
INS NM_000207.2 -?/. - c.-4161G>A - r.(?) p.(=)
TH NM_000360.3 -?/. - c.1255G>A - r.(?) p.(Val419Met)
IGF2 NM_000612.4 -?/. - c.-27089G>A - r.(?) p.(=)
INS-IGF2 NM_001042376.2 -?/. - c.-4161G>A - r.(?) p.(=)
TH NM_199292.2 -?/. - c.1348G>A - r.(?) p.(Val450Met)