Variant #0000866729 (NC_000022.10:g.19960542G>C, NM_000754.3:c.*4283G>C (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.19960542G>C
DNA change (hg38) -
Published as ARVCF(NM_001670.2):c.2456C>G (p.A819G)
ISCN -
DB-ID ARVCF_000031
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) 1.0E-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 2022-05-09 16:01:56 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
COMT NM_000754.3 ?/. - c.*4283G>C r.(=) p.(=)
ARVCF NM_001670.2 ?/. - c.2456C>G r.(?) p.(Ala819Gly)
TXNRD2 NM_006440.3 ?/. - c.-31216C>G r.(?) p.(=)


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