Variant #0000274321 (NC_000022.10:g.19951804G>A, NM_000754.3:c.597G>A (COMT))

Chromosome 22
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.19951804G>A
DNA change (hg38) g.19964281G>A
Published as COMT(NM_000754.3):c.597G>A (p.P199=)
ISCN -
DB-ID COMT_000003
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) 0.02973 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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-07-17 10:51:13 +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.597G>A r.(?) p.(Pro199=)
ARVCF NM_001670.2 -/. - c.*6475C>T r.(=) p.(=)
TXNRD2 NM_006440.3 -/. - c.-22478C>T r.(?) p.(=)


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