Variant #0000972169 (NC_000003.11:g.24231580C>T, NM_000461.4:c.268G>A (THRB))

Chromosome 3
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.24231580C>T
DNA change (hg38) -
Published as -
ISCN -
DB-ID THRB_000023
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs1428476390
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner MobiDetails
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by MobiDetails
Date created 2024-04-09 15:48:01 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
THRB NM_000461.4 ?/. - c.268G>A r.(?) p.(Glu90Lys)


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