Variant #0000693059 (NC_000021.8:g.45657073A>G, NM_015259.4:c.83T>C (ICOSLG))

Chromosome 21
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.45657073A>G
DNA change (hg38) -
Published as ICOSLG(NM_001365759.1):c.2T>C (p.M1?), ICOSLG(NM_015259.5):c.83T>C (p.M28T)
ISCN -
DB-ID ICOSLG_000002
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) 1.0E-5 View details
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 2024-02-26 20:06:56 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ICOSLG NM_015259.4 ?/. - c.83T>C r.(?) p.(Met28Thr)


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