Variant #0001002526 (NC_000016.9:g.70557392G>A, NM_015386.2:c.55C>T (COG4))

Chromosome 16
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.70557392G>A
DNA change (hg38) -
Published as COG4(NM_001195139.1):c.55C>T (p.(Gln19*))
ISCN -
DB-ID SF3B3_000005
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2024-08-28 13:16:32 +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     
SF3B3 NM_012426.4 +?/. - c.-510G>A r.(?) p.(=)
COG4 NM_015386.2 +?/. - c.55C>T r.(?) p.(Gln19*)


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