Variant #0000533781 (NC_000008.10:g.133899448_133899458del, NM_003235.4:c.1831_1841del (TG))

Chromosome 8
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.133899448_133899458del
DNA change (hg38) g.132887203_132887213del
Published as TG(NM_003235.5):c.1831_1841delACACCTGAAAG (p.T611Afs*13)
ISCN -
DB-ID TG_000101
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_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SLA NM_001045556.2 +/. - c.*151313_*151323del r.(=) p.(=)
TG NM_003235.4 +/. - c.1831_1841del r.(?) p.(Thr611AlafsTer13)


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