Variant #0001005911 (NC_000022.10:g.20030957_20030958insC, NM_152906.4:c.136_137insC (TANGO2))

Chromosome 22
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.20030957_20030958insC
DNA change (hg38) -
Published as TANGO2(NM_152906.4):c.136_137insC (p.(Ile46fs))
ISCN -
DB-ID TANGO2_000023
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 2024-08-28 13:16:32 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TANGO2 NM_152906.4 +/. - c.136_137insC r.(?) p.(Ile46Thrfs*45)


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