Variant #0000930889 (NC_000017.10:g.7460572C>T, NM_003809.2:c.655C>T (TNFSF12))

Chromosome 17
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.7460572C>T
DNA change (hg38) -
Published as TNFSF12(NM_003809.3):c.655C>T (p.R219W)
ISCN -
DB-ID EIF4A1_000009
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) 2.0E-5 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2023-07-07 10:10:56 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
EIF4A1 NM_001416.3 ?/. - c.-15588C>T r.(?) p.(=)
TNFSF13 NM_003808.3 ?/. - c.-1785C>T r.(?) p.(=)
TNFSF12 NM_003809.2 ?/. - c.655C>T r.(?) p.(Arg219Trp)
SENP3 NM_015670.5 ?/. - c.-5020C>T r.(?) p.(=)
TNFSF12-TNFSF13 NM_172089.3 ?/. - c.498+353C>T r.(=) p.(=)


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