Variant #0000889760 (NC_000011.9:g.2188229G>T, NM_199292.2:c.822C>A (TH))

Chromosome 11
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.2188229G>T
DNA change (hg38) -
Published as TH(NM_199292.3):c.822C>A (p.Y274*)
ISCN -
DB-ID TH_000082
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_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2022-11-01 13:01:21 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TH NM_000360.3 +/. - c.729C>A r.(?) p.(Tyr243*)
TH NM_199292.2 +/. - c.822C>A r.(?) p.(Tyr274*)


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