Variant #0000950200 (NC_000014.8:g.104501396A>G, NC_000014.8(NM_153046.2):c.3716+3A>G (TDRD9))

Chromosome 14
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.104501396A>G
DNA change (hg38) -
Published as -
ISCN -
DB-ID RD3L_000002
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) 0.0003 View details
Owner VKGL-NL_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2023-11-27 17:35:39 +01:00 (CET)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
RD3L NM_001257268.1 ?/. - c.-92975T>C r.(?) p.(=)
TDRD9 NM_153046.2 ?/. - c.3716+3A>G r.spl? p.?


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