Variant #0000854433 (NC_000016.9:g.23647713T>G, NC_000016.9(NM_024675.3):c.212-58A>C (PALB2))

Chromosome 16
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.23647713T>G
DNA change (hg38) -
Published as PALB2(NM_024675.3):c.212-58A>C
ISCN -
DB-ID PALB2_010023 See all 15 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) Retrieve
Owner VKGL-NL_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2022-05-09 15:47:41 +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     

Haplotype     
PALB2 NM_024675.3 -/. - c.212-58A>C r.(=) p.(=) -
DCTN5 NM_032486.3 -/. - c.-5151T>G r.(?) p.(=) -


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