Variant #0000680989 (NC_000017.10:g.65955782_65955783insGCCCCTCCAGCCCCTCCAGCCCCTCCA, NM_004459.6:c.8001_8002insGCCCCTCCAGCCCCTCCAGCCCCTCCA (BPTF))

Chromosome 17
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.65955782_65955783insGCCCCTCCAGCCCCTCCAGCCCCTCCA
DNA change (hg38) -
Published as BPTF(NM_004459.7):c.8001_8002insGCCCCTCCAGCCCCTCCAGCCCCTCCA (p.A2659_P2667dup)
ISCN -
DB-ID BPTF_000034
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 2020-08-06 14:59:34 +02:00 (CEST)
Date last edited 2021-09-17 14:40:49 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
BPTF NM_004459.6 -?/. - c.8001_8002insGCCCCTCCAGCCCCTCCAGCCCCTCCA r.(?) p.(Ala2659_Pro2667dup)


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.