Variant #0000571362 (NC_000022.10:g.19929268T>C, NM_000754.3:c.-244T>C (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.19929268T>C
DNA change (hg38) g.19941745T>C
Published as TXNRD2(NM_001282512.2):c.59A>G (p.Q20R)
ISCN -
DB-ID ARVCF_000016
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_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 10:49:43 +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.-244T>C r.(?) p.(=)
ARVCF NM_001670.2 -?/. - c.*29011A>G r.(=) p.(=)
TXNRD2 NM_006440.3 -?/. - c.59A>G r.(?) p.?


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