Variant #0000531578 (NC_000007.13:g.19156653_19156671dup, NM_000474.3:c.276_294dup (TWIST1))

Chromosome 7
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.19156653_19156671dup
DNA change (hg38) g.19117030_19117048dup
Published as TWIST1(NM_000474.3):c.276_294dupCAGCAGCAGCGGCGGCGGG (p.S99Qfs*145)
ISCN -
DB-ID TWIST1_000057
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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-06-22 14:43:03 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TWIST1 NM_000474.3 -/. - c.276_294dup r.(?) p.(Ser99GlnfsTer145)


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