Variant #0000248339 (NC_000016.9:g.23646857A>G, NM_024675.3:c.1010T>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.23646857A>G
DNA change (hg38) g.23635536A>G
Published as PALB2(NM_024675.3):c.1010T>C (p.(Leu337Ser), p.L337S), PALB2(NM_024675.4):c.1010T>C (p.L337S)
ISCN -
DB-ID PALB2_010059 See all 34 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) 0.01489 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2018-01-15 20:58:59 +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.1010T>C r.(?) p.(Leu337Ser) -


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