Variant #0000562842 (NC_000017.10:g.65889832_65889833insTGAT, NM_004459.6:c.2780_2781insTGAT (BPTF))

Chromosome 17
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.65889832_65889833insTGAT
DNA change (hg38) g.67893716_67893717insTGAT
Published as BPTF(NM_182641.4):c.2402_2403insTGAT (p.S802Dfs*4)
ISCN -
DB-ID BPTF_000020
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_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-07-14 10:45:56 +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.2780_2781insTGAT r.(?) p.(Ser928AspfsTer4)


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