Variant #0000948975 (NC_000007.13:g.98552729_98552730del, NM_001244580.1:c.5718_5719del (TRRAP))

Chromosome 7
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.98552729_98552730del
DNA change (hg38) -
Published as TRRAP(NM_003496.4):c.5664_5665delTA (p.H1888Qfs*105)
ISCN -
DB-ID TRRAP_000077
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 2023-11-27 17:35:39 +01:00 (CET)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TRRAP NM_001244580.1 ?/. - c.5718_5719del r.(?) p.(His1906Glnfs*105)


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