Variant #0001047558 (NC_000016.9:g.23649405G>C, NM_024675.3:c.94C>G (PALB2))

Chromosome 16
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.23649405G>C
DNA change (hg38) -
Published as -
ISCN -
DB-ID PALB2_010178 See all 7 reported entries
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs151316635
Origin Unknown
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 2.0E-5 View details
Owner MobiDetails
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by MobiDetails
Date created 2025-08-28 15:53:01 +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.94C>G r.(?) p.(Leu32Val) -


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