Variant #0000892872 (NC_000016.9:g.23649211_23649214del, NM_024675.3:c.172_175del (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.23649211_23649214del
DNA change (hg38) -
Published as PALB2(NM_024675.3):c.172_175del (p.(Gln60Argfs*7)), PALB2(NM_024675.3):c.172_175delTTGT (p.Q60Rfs*7), PALB2(NM_024675.4):c.172_175delTTGT (p.Q60Rfs*7)
ISCN -
DB-ID PALB2_010002 See all 19 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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2022-11-01 13:41:49 +01:00 (CET)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

Haplotype     
PALB2 NM_024675.3 +/. - c.172_175del r.(?) p.(Gln60ArgfsTer7) -
DCTN5 NM_032486.3 +/. - c.-3653_-3650del r.(?) p.(=) -


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