Variant #0000862638 (NC_000011.9:g.65835675G>A, NM_018026.3:c.-2283G>A (PACS1))

Chromosome 11
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.65835675G>A
DNA change (hg38) -
Published as SF3B2(NM_006842.3):c.2487G>A (p.A829=)
ISCN -
DB-ID PACS1_000024
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) 0.00256 View details
Owner VKGL-NL_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2022-05-09 15:51:19 +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     
SF3B2 NM_006842.2 -/. - c.2487G>A r.(?) p.(Ala829=)
PACS1 NM_018026.3 -/. - c.-2283G>A r.(?) p.(=)


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