Variant #0000545394 (NC_000011.9:g.67397304_67397320del, NM_005995.4:c.*1757_*1773del (TBX10))

Chromosome 11
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.67397304_67397320del
DNA change (hg38) g.67629833_67629849del
Published as NUDT8(NM_181843.2):c.64_80delACGGCCCGGCTCCGCGC (p.T22Afs*48)
ISCN -
DB-ID NUDT8_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_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 2020-07-01 09:49:32 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TBX10 NM_005995.4 ?/. - c.*1757_*1773del r.(=) p.(=)
NUDT8 NM_181843.2 ?/. - c.64_80del r.(?) p.(Thr22AlafsTer48)


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