Variant #0000689615 (NC_000006.11:g.123786042del, NC_000006.11(NM_006073.3):c.931+18del (TRDN))

Chromosome 6
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.123786042del
DNA change (hg38) -
Published as TRDN(NM_001256020.1):c.889delT (p.S297Lfs*8), TRDN(NM_001256020.2):c.889delT (p.S297Lfs*8), TRDN-AS1(NR_110844.1):n.175-3919delA
ISCN -
DB-ID TRDN_000011 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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2020-09-15 15:50:26 +02:00 (CEST)
Date last edited 2023-04-16 21:50:28 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

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


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