Variant #0000527096 (NC_000006.11:g.123892246_123892249del, NM_006073.3:c.53_56del (TRDN))

Chromosome 6
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.123892246_123892249del
DNA change (hg38) g.123571101_123571104del
Published as TRDN(NM_006073.4):c.53_56delACAG (p.D18Afs*14)
ISCN -
DB-ID TRDN_000001 See all 3 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_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     
TRDN NM_001251987.1 +?/. - c.53_56del r.(?) p.(Asp18AlafsTer14)
TRDN NM_006073.3 +?/. - c.53_56del r.(?) p.(Asp18AlafsTer14)


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