Variant #0000984109 (NC_000022.10:g.19867758A>G, NM_000754.3:c.-61754A>G (COMT))

Chromosome 22
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.19867758A>G
DNA change (hg38) -
Published as TXNRD2(NM_006440.5):c.1219T>C (p.(Cys407Arg))
ISCN -
DB-ID COMT_000034
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 2024-04-19 20:27:30 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
COMT NM_000754.3 ?/. - c.-61754A>G r.(?) p.(=)
TXNRD2 NM_006440.3 ?/. - c.1219T>C r.(?) p.?


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