Variant #0000806771 (NC_000015.9:g.55631510del, NM_004855.4:c.840del (PIGB))

Chromosome 15
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.55631510del
DNA change (hg38) -
Published as PIGB(NM_004855.5):c.840delT (p.F280Lfs*12)
ISCN -
DB-ID CCPG1_000012
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_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2021-09-17 14:40:49 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CCPG1 NM_004748.4 ?/. - c.*20194del r.(?) p.(=)
PIGB NM_004855.4 ?/. - c.840del r.(?) p.(Phe280Leufs*12)


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