Variant #0000689640 (NC_000006.11:g.139694968_139694970del, NM_001168388.2:c.117_119del (CITED2))

Chromosome 6
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.139694968_139694970del
DNA change (hg38) -
Published as CITED2(NM_006079.4):c.117_119delCCA (p.(His39del)), CITED2(NM_006079.4):c.117_119delCCA (p.H39del), CITED2(NM_006079.5):c.117_119delCCA (p.H39del)
ISCN -
DB-ID CITED2_000007 See all 5 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) 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 2024-08-28 13:16:32 +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.117_119del r.(?) p.(His39del)


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