Variant #0000968260 (NC_000016.9:g.23614792G>C, NM_024675.3:c.3549C>G (PALB2))

Chromosome 16
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.23614792G>C
DNA change (hg38) -
Published as PALB2(NM_024675.3):c.3549C>G (p.(Tyr1183Ter)), PALB2(NM_024675.4):c.3549C>G (p.Y1183*)
ISCN -
DB-ID PALB2_000008 See all 17 reported entries
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) 2.0E-5 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 2024-02-26 20:06:56 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

Haplotype     
PALB2 NM_024675.3 +/. - c.3549C>G r.(?) p.(Tyr1183*) -


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