Variant #0000720653 (NC_000006.11:g.123759284A>C, NC_000006.11(NM_006073.3):c.992-17T>G (TRDN))

Chromosome 6
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.123759284A>C
DNA change (hg38) -
Published as TRDN(NM_006073.4):c.992-17T>G
ISCN -
DB-ID TRDN_000110
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) 0.00011 View details
Owner VKGL-NL_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2021-02-08 18:36:18 +01:00 (CET)
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.992-14T>G r.(=) p.(=)
TRDN NM_006073.3 -?/. - c.992-17T>G r.(=) p.(=)


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