Variant #0000613575 (NC_000011.9:g.65838073_65838078dup, NM_018026.3:c.116_121dup (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.65838073_65838078dup
DNA change (hg38) g.66070602_66070607dup
Published as PACS1(NM_018026.3):c.101_102insGCAGCA (p.(Gln39_Gln40dup))
ISCN -
DB-ID PACS1_000019
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 2019-12-04 15:24:38 +01:00 (CET)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SF3B2 NM_006842.2 -?/. - c.*1857_*1862dup r.(=) p.(=)
PACS1 NM_018026.3 -?/. - c.116_121dup r.(?) p.(Gln39_Gln40dup)


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