Variant #0000689344 (NC_000004.11:g.76927406C>A, NM_001179.5:c.-68576C>A (ART3))

Chromosome 4
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.76927406C>A
DNA change (hg38) -
Published as CXCL9(NM_002416.2):c.86G>T (p.G29V)
ISCN -
DB-ID ART3_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 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 N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ART3 NM_001179.5 ?/. - c.-68576C>A r.(?) p.(=)
CXCL10 NM_001565.3 ?/. - c.*15677G>T r.(=) p.(=)
CXCL9 NM_002416.1 ?/. - c.86G>T r.(?) p.(Gly29Val)
CXCL11 NM_005409.4 ?/. - c.*28540G>T r.(=) p.(=)
SDAD1 NM_018115.2 ?/. - c.-15412G>T r.(?) p.(=)


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