Variant #0000983220 (NC_000019.9:g.13216393_13216394del, NM_002501.2:c.*10965_*10966del (NFIX))

Chromosome 19
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.13216393_13216394del
DNA change (hg38) -
Published as TRMT1(NM_001136035.2):c.1610_1611delAA (p.(Glu537fs))
ISCN -
DB-ID LYL1_000004
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2024-04-19 20:27:30 +02:00 (CEST)
Date last edited 2024-08-28 13:16:32 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TRMT1 NM_001136035.2 ?/. - c.1610_1611del r.(?) p.(Glu537Glyfs*17)
NFIX NM_002501.2 ?/. - c.*10965_*10966del r.(=) p.(=)
LYL1 NM_005583.4 ?/. - c.-3074_-3073del r.(?) p.(=)


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