Variant #0001037722 (NC_000010.10:g.112660195dup, NM_014456.4:c.*2349dup (PDCD4))

Chromosome 10
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.112660195dup
DNA change (hg38) -
Published as BBIP1(NM_001195305.3):c.205dup (p.(Met69Asnfs*29))
ISCN -
DB-ID PDCD4_000004
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 2025-05-05 21:14:00 +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     
BBIP1 NM_001195304.1 ?/. - c.*50dup r.(?) p.(=)
BBIP1 NM_001195305.1 ?/. - c.205dup r.(?) p.(Met69Asnfs*29)
PDCD4 NM_014456.4 ?/. - c.*2349dup r.(?) p.(=)


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