Variant #0000693109 (NC_000022.10:g.19969030G>A, NM_000754.3:c.*12771G>A (COMT))

Chromosome 22
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.19969030G>A
DNA change (hg38) -
Published as ARVCF(NM_001670.2):c.600C>T (p.S200=)
ISCN -
DB-ID ARVCF_000027
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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2020-09-15 15:50:26 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
COMT NM_000754.3 -?/. - c.*12771G>A r.(=) p.(=)
ARVCF NM_001670.2 -?/. - c.600C>T r.(?) p.(Ser200=)


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