Genomic variant #0000044632

Individual ID 00022368
Chromosome 16
Allele Parent #1
Affects function (as reported) Affects function
Affects function (by curator) Affects function
DNA change (genomic) (Relative to hg19 / GRCh37) g.23634324G>A
DNA change (hg38) g.23623003G>A
Published as -
ISCN -
DB-ID PALB2_000013 See all 7 reported entries
Variant remarks -
Reference PubMed: Reid 2007
ClinVar ID -
dbSNP ID rs118203999
Origin Unknown
Segregation ?
Frequency -
Re-site -
VIP 0
Methylation -
Average frequency (large NGS studies) Variant not found in online data sets
Owner Arleen D. Auerbach




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

ClassClinical     

RNA change     

Protein     

Haplotype     
PALB2 NM_024675.3 +/+ 9 c.2962C>T pathogenic r.(?) p.(Gln988*) FA



Screenings


AscendingScreening ID     

Template     

Technique     

Tissue     

Remarks     

Genes screened     

Variants found     

Owner     
0000022366 DNA SEQ - - PALB2 2 Arleen D. Auerbach