Variant #0000616078 (NC_000016.9:g.67964625_67964626del, NM_002801.3:c.*3838_*3839del (PSMB10))

Chromosome 16
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.67964625_67964626del
DNA change (hg38) g.67930722_67930723del
Published as CTRL(NM_001907.2):c.318+4_318+5del (p.?)
ISCN -
DB-ID CTRL_000005
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 2019-12-04 15:24:38 +01:00 (CET)
Date last edited 2020-07-09 18:07:21 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CTRL NM_001907.2 ?/. - c.318+4_318+5del r.spl? p.?
PSMB10 NM_002801.3 ?/. - c.*3838_*3839del r.(=) p.(=)
PSKH1 NM_006742.2 ?/. - c.*3080_*3081del r.(=) p.(=)


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