Variant #0000690646 (NC_000010.10:g.112660164C>T, NM_014456.4:c.*2318C>T (PDCD4))

Chromosome 10
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.112660164C>T
DNA change (hg38) -
Published as BBIP1(NM_001195305.2):c.233G>A (p.R78H), BBIP1(NM_001195305.3):c.233G>A (p.R78H)
ISCN -
DB-ID BBIP1_000001 See all 2 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) 6.0E-5 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2020-09-15 15:50:26 +02:00 (CEST)
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     
BBIP1 NM_001195304.1 -?/. - c.*78G>A r.(=) p.(=)
BBIP1 NM_001195305.1 -?/. - c.233G>A r.(?) p.(Arg78His)
PDCD4 NM_014456.4 -?/. - c.*2318C>T r.(=) p.(=)


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