Variant #0000518686 (NC_000003.11:g.184091392_184091393insGAAG, NC_000003.11(NM_000460.2):c.229-21_229-20insTCCT (THPO))

Chromosome 3
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.184091392_184091393insGAAG
DNA change (hg38) g.184373604_184373605insGAAG
Published as THPO(NM_000460.4):c.229-21_229-20insTCCT
ISCN -
DB-ID THPO_000008
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_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2021-09-17 14:40:49 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
THPO NM_000460.2 -/. - c.229-21_229-20insTCCT r.(=) p.(=)


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