Variant #0001045046 (NC_000016.9:g.23649452T>A, NC_000016.9(NM_024675.3):c.49-2A>T (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.23649452T>A
DNA change (hg38) -
Published as -
ISCN -
DB-ID PALB2_010325 See all 4 reported entries
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs786203245
Origin Unknown
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner MobiDetails
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by MobiDetails
Date created 2025-05-23 13:47:01 +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.49-2A>T r.(?) p.(?) -


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