Variant #0000263739 (NC_000017.10:g.65822394_65822396del, NM_004459.6:c.554_556del (BPTF))

Chromosome 17
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.65822394_65822396del
DNA change (hg38) g.67826278_67826280del
Published as BPTF(NM_182641.3):c.554_556delACG (p.(Asp185del)), BPTF(NM_182641.4):c.554_556delACG (p.D185del)
ISCN -
DB-ID BPTF_000013 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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2024-08-28 13:16:32 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
BPTF NM_004459.6 -/. - c.554_556del r.(?) p.(Asp185del)


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