Variant #0000328888 (NC_000022.10:g.19969136C>T, NM_000754.3:c.*12877C>T (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.19969136C>T
DNA change (hg38) g.19981613C>T
Published as ARVCF(NM_001670.2):c.494G>A (p.(Arg165Gln))
ISCN -
DB-ID ARVCF_000013
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) 9.0E-5 View details
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)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
COMT NM_000754.3 ?/. - c.*12877C>T r.(=) p.(=)
ARVCF NM_001670.2 ?/. - c.494G>A r.(?) p.(Arg165Gln)


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