Variant #0000676056 (NC_000002.11:g.162273117_162273120del, NM_006593.2:c.196_199del (TBR1))

Chromosome 2
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.162273117_162273120del
DNA change (hg38) -
Published as TBR1(NM_006593.4):c.196_199delGACA (p.D66Ifs*149)
ISCN -
DB-ID PSMD14_000001
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)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PSMD14 NM_005805.5 +/. - c.*5206_*5209del r.(=) p.(=)
TBR1 NM_006593.2 +/. - c.196_199del r.(?) p.(Asp66IlefsTer149)


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