Variant #0000571356 (NC_000022.10:g.19898935A>C, NM_000754.3:c.-30577A>C (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.19898935A>C
DNA change (hg38) g.19911412A>C
Published as TXNRD2(NM_006440.3):c.627T>G (p.D209E)
ISCN -
DB-ID COMT_000014
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) 1.0E-5 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-07-17 10:44:28 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
COMT NM_000754.3 ?/. - c.-30577A>C r.(?) p.(=)
TXNRD2 NM_006440.3 ?/. - c.627T>G r.(?) p.?


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