Variant #0000571346 (NC_000022.10:g.19868172C>G, NM_000754.3:c.-61340C>G (COMT))

Chromosome 22
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.19868172C>G
DNA change (hg38) g.19880649C>G
Published as TXNRD2(NM_006440.3):c.1155G>C (p.G385=)
ISCN -
DB-ID COMT_000009
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) 2.0E-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 10:39:24 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
COMT NM_000754.3 -?/. - c.-61340C>G r.(?) p.(=)
TXNRD2 NM_006440.3 -?/. - c.1155G>C r.(?) p.?


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