Variant #0000915491 (NC_000022.10:g.23653976_23653979dup, NM_004327.3:c.3275_3278dup (BCR))

Chromosome 22
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.23653976_23653979dup
DNA change (hg38) -
Published as BCR(NM_004327.3):c.3274_3275insCCGG (p.(Val1094ArgfsTer17)), BCR(NM_004327.3):c.3275_3278dupCCGG (p.V1094Rfs*17), BCR(NM_004327.4):c.3275_3278dupCC...
ISCN -
DB-ID BCR_000014 See all 3 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) 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 2023-01-11 15:44:22 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
BCR NM_004327.3 ?/. - c.3275_3278dup r.(?) p.(Val1094ArgfsTer17)


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