Variant #0000513971 (NC_000002.11:g.204820511_204820520del, NM_012092.3:c.211_220del (ICOS))

Chromosome 2
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.204820511_204820520del
DNA change (hg38) g.203955788_203955797del
Published as ICOS(NM_012092.3):c.211_220delAGTGGAAACA (p.S71Qfs*7)
ISCN -
DB-ID ICOS_000004
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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-08-06 14:59:34 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ICOS NM_012092.3 ?/. - c.211_220del r.(?) p.(Ser71GlnfsTer7)


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