Variant #0001038398 (NC_000011.9:g.2189814C>T, NM_199292.2:c.487G>A (TH))

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.2189814C>T
DNA change (hg38) -
Published as TH(NM_000360.4):c.394G>A (p.(Val132Met)), TH(NM_199292.2):c.487G>A (p.V163M)
ISCN -
DB-ID TH_000051 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) 5.0E-5 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2025-05-05 21:14:00 +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     
TH NM_000360.3 ?/. - c.394G>A r.(?) p.(Val132Met)
TH NM_199292.2 ?/. - c.487G>A r.(?) p.(Val163Met)


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