Variant #0000948638 (NC_000006.11:g.123696746A>G, NC_000006.11(NM_006073.3):c.1273+4T>C (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.123696746A>G
DNA change (hg38) -
Published as TRDN(NM_006073.4):c.1273+4T>C
ISCN -
DB-ID TRDN_000126 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) 1.0E-5 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2023-11-27 17:35:39 +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.1276+4T>C r.spl? p.?
TRDN NM_006073.3 ?/. - c.1273+4T>C r.spl? p.?


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