Variant #0000655285 (NC_000005.9:g.137507118_137507120del, NC_000005.9(NM_006696.3):c.187-8_187-6del (BRD8))

Chromosome 5
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.137507118_137507120del
DNA change (hg38) g.138171429_138171431del
Published as BRD8(NM_139199.2):c.187-8_187-6delTTT
ISCN -
DB-ID BRD8_000014 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) Retrieve
Owner VKGL-NL_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2020-03-23 16:13:27 +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     
BRD8 NM_006696.3 -/. - c.187-8_187-6del r.(=) p.(=)


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