Variant #0000656705 (NC_000011.9:g.118220583A>T, NM_000073.2:c.205A>T (CD3G))

Chromosome 11
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.118220583A>T
DNA change (hg38) g.118349868A>T
Published as CD3G(NM_000073.2):c.205A>T (p.K69*)
ISCN -
DB-ID CD3G_000005 See all 2 reported entries
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) 8.0E-5 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2020-03-23 16:13:27 +01:00 (CET)
Date last edited 2020-07-01 15:22:50 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CD3G NM_000073.2 +?/. - c.205A>T r.(?) p.(Lys69Ter)


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