Variant #0000315162 (NC_000022.10:g.19906370G>A, NM_000754.3:c.-23142G>A (COMT))

Chromosome 22
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.19906370G>A
DNA change (hg38) g.19918847G>A
Published as TXNRD2(NM_006440.3):c.374+13C>T, TXNRD2(NM_006440.5):c.374+13C>T
ISCN -
DB-ID TXNRD2_000040 See all 2 reported entries
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) 0.03185 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
COMT NM_000754.3 -/. - c.-23142G>A r.(?) p.(=)
TXNRD2 NM_006440.3 -/. - c.374+13C>T r.(=) p.(=)


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