Variant #0000172734 (NC_000017.10:g.65889796del, NM_004459.6:c.2744del (BPTF))

Chromosome 17
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Affects function
Classification method ACMG
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.65889796del
DNA change (hg38) g.67893680del
Published as -
ISCN -
DB-ID BPTF_000011
Variant remarks -
Reference PubMed: Stankiewicz 2017, Journal: Stankiewicz 2017
ClinVar ID -
dbSNP ID -
Origin De novo
Segregation yes
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Bernt Popp
Database submission license No license selected
Created by Bernt Popp
Date created 2017-07-02 23:55:59 +02:00 (CEST)
Date last edited 2017-11-17 15:02:09 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
BPTF NM_004459.6 +/+ 8 c.2744del r.(?) p.(Asn915Thrfs*36)



Screenings

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