Variant #0000999297 (NC_000011.9:g.65835811G>A, NM_018026.3:c.-2147G>A (PACS1))

Chromosome 11
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.65835811G>A
DNA change (hg38) -
Published as SF3B2(NM_006842.2):c.2616+7G>A (p.?)
ISCN -
DB-ID PACS1_000037
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) 0.00053 View details
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     
SF3B2 NM_006842.2 -?/. - c.2616+7G>A r.(=) p.(=)
PACS1 NM_018026.3 -?/. - c.-2147G>A r.(?) p.(=)


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