Variant #0000658882 (NC_000022.10:g.19951742A>T, NM_000754.3:c.535A>T (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.19951742A>T
DNA change (hg38) g.19964219A>T
Published as COMT(NM_000754.3):c.535A>T (p.K179*), COMT(NM_001362828.2):c.535A>T (p.K179*)
ISCN -
DB-ID COMT_000002 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) 2.0E-5 View details
Owner VKGL-NL_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2020-03-23 16:13:27 +01:00 (CET)
Date last edited 2020-07-17 10:51:00 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
COMT NM_000754.3 ?/. - c.535A>T r.(?) p.(Lys179Ter)
ARVCF NM_001670.2 ?/. - c.*6537T>A r.(=) p.(=)
TXNRD2 NM_006440.3 ?/. - c.-22416T>A r.(?) p.(=)


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.