Variant #0000329343 (NC_000003.11:g.42251604_42251609dup, NM_014965.4:c.1916_1921dup (TRAK1))

Chromosome 3
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.42251604_42251609dup
DNA change (hg38) g.42210112_42210117dup
Published as TRAK1(NM_001265608.1):c.2066_2067insGGAGGA (p.(Glu689_Glu690insGluGlu)), TRAK1(NM_001265608.1):c.2090_2095dupAGGAGG (p.E697_E698dup)
ISCN -
DB-ID TRAK1_000006 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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2024-04-19 20:27:30 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TRAK1 NM_014965.4 ?/. - c.1916_1921dup r.(?) p.(Glu639_Glu640dup)


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