Variant #0000681784 (NC_000022.10:g.19950045T>A, NC_000022.10(NM_000754.3):c.1-5T>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.19950045T>A
DNA change (hg38) -
Published as COMT(NM_001362828.2):c.-5T>A
ISCN -
DB-ID ARVCF_000026
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_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2020-08-06 14:59:34 +02:00 (CEST)
Date last edited 2021-09-17 14:40:49 +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.1-5T>A r.spl? p.?
ARVCF NM_001670.2 ?/. - c.*8234A>T r.(=) p.(=)
TXNRD2 NM_006440.3 ?/. - c.-20719A>T r.(?) p.(=)


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