Variant #0000610045 (NC_000006.11:g.136603827_136603828insGACACGCCGAATCGCGGTTACGGGAATTTATCTCCGTTGCAACCACACAGCGGCCATTTCCCG, NC_000006.11(NM_014739.2):c.-114-3_-114-2insCGGGAAATGGCCGCTGTGTGGTTGCAACGGAGATAAATTCCCGTAACCGCGATTCGGCGTGTC (BCLAF1))

Chromosome 6
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.136603827_136603828insGACACGCCGAATCGCGGTTACGGGAATTTATCTCCGTTGCAACCACACAGCGGCCATTTCCCG
DNA change (hg38) g.136282689_136282690insGACACGCCGAATCGCGGTTACGGGAATTTATCTCCGTTGCAACCACACAGCGGCCATTTCCCG
Published as BCLAF1(NM_001077440.1):c.-114-3_-114-2insCGGGAAATGGCCGCTGTGTGGTTGCAACGGAGATAAATTCCCGTAACCGCGATTCGGCGTGTC (p.(=))
ISCN -
DB-ID BCLAF1_000025
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 2020-06-22 10:27:31 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
BCLAF1 NM_014739.2 -?/. - c.-114-3_-114-2insCGGGAAATGGCCGCTGTGTGGTTGCAACGGAGATAAATTCCCGTAACCGCGATTCGGCGTGTC r.spl? p.?


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