Variant #0000328885 (NC_000022.10:g.19960805G>A, NM_000754.3:c.*4546G>A (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.19960805G>A
DNA change (hg38) g.19973282G>A
Published as ARVCF(NM_001670.2):c.2275C>T (p.(Arg759Cys))
ISCN -
DB-ID ARVCF_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) Retrieve
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
COMT NM_000754.3 ?/. - c.*4546G>A r.(=) p.(=)
ARVCF NM_001670.2 ?/. - c.2275C>T r.(?) p.(Arg759Cys)
TXNRD2 NM_006440.3 ?/. - c.-31479C>T r.(?) p.(=)


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