Variant #0000527078 (NC_000006.11:g.123786042dup, NC_000006.11(NM_006073.3):c.931+18dup (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.123786042dup
DNA change (hg38) g.123464897dup
Published as TRDN(NM_001256020.2):c.889dupT (p.S297Ffs*32)
ISCN -
DB-ID TRDN_000073
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 2020-03-23 16:13:27 +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.931+18dup r.(=) p.(=)
TRDN NM_006073.3 -/. - c.931+18dup r.(=) p.(=)


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