Variant #0000266816 (NC_000006.11:g.139694502_139694507del, NM_001168388.2:c.580_585del (CITED2))

Chromosome 6
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.139694502_139694507del
DNA change (hg38) g.139373365_139373370del
Published as CITED2(NM_006079.5):c.580_585delGGCGGC (p.G194_G195del)
ISCN -
DB-ID CITED2_000001
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) 0.00127 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2018-01-15 20:58:59 +01:00 (CET)
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     
CITED2 NM_001168388.2 -/. - c.580_585del r.(?) p.(Gly194_Gly195del)


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