Variant #0000983221 (NC_000019.9:g.13216396_13216408del, NM_002501.2:c.*10968_*10980del (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.13216396_13216408del
DNA change (hg38) -
Published as TRMT1(NM_001136035.2):c.1596_1608delCTTCACCATCCGG (p.(Asn532fs))
ISCN -
DB-ID LYL1_000005
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)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TRMT1 NM_001136035.2 ?/. - c.1596_1608del r.(?) p.(Asn532Lysfs*123)
NFIX NM_002501.2 ?/. - c.*10968_*10980del r.(=) p.(=)
LYL1 NM_005583.4 ?/. - c.-3088_-3076del r.(?) p.(=)


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.