Variant #0001052481 (NC_000006.11:g.123786042dup, NC_000006.11(NM_006073.3):c.931+18dup (TRDN))

Chromosome 6
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.123786042dup
DNA change (hg38) -
Published as TRDN(NM_001256020.2):c.889dup (p.(*297Phefs*32)), TRDN(NM_001256020.2):c.889dupT (p.S297Ffs*32)
ISCN -
DB-ID TRDN_000073 See all 2 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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2025-11-01 13:22:20 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TRDN NM_001251987.1 ?/. - c.931+18dup r.(=) p.(=)
TRDN NM_006073.3 ?/. - c.931+18dup r.(=) p.(=)


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