Variant #0000982814 (NC_000017.10:g.7460608T>C, NM_003809.2:c.691T>C (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.7460608T>C
DNA change (hg38) -
Published as TNFSF12(NM_003809.3):c.691T>C (p.W231R)
ISCN -
DB-ID EIF4A1_000010
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) Retrieve
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2024-04-19 20:27:30 +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.-15552T>C r.(?) p.(=)
TNFSF13 NM_003808.3 ?/. - c.-1749T>C r.(?) p.(=)
TNFSF12 NM_003809.2 ?/. - c.691T>C r.(?) p.(Trp231Arg)
SENP3 NM_015670.5 ?/. - c.-4984T>C r.(?) p.(=)
TNFSF12-TNFSF13 NM_172089.3 ?/. - c.498+389T>C r.(=) p.(=)


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