Variant #0000001566 (NC_000001.11:g.173257056T>G, NM_003326.4:c.-49880A>C (TNFSF4))

Individual ID 00000335
Chromosome 1
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg38 / GRCh38) g.173257056T>G
Published as -
Reference K H Chua et al. (2016), dbSNP
DB-ID TNFSF4_000002 See all 6 reported entries
dbSNP ID rs704840
Frequency 11/31
Variant remarks -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Nuur Athirah Binti Mohd Daud
Database submission license Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 InternationalCreative Commons License
Created by Nuur Athirah Binti Mohd Daud
Date created 2021-01-07 11:39:30 +08:00 (CST)
Date last edited 2021-09-01 14:40:24 +08:00 (CST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

Published as     

RNA change     

Protein     

GVS function     

Clinical classification     
TNFSF4 NM_003326.4 +/. - c.-49880A>C - r.(=) p.(=) - -



Screenings


AscendingScreening ID     

Template     

Technique     

Genes screened     

Variants found     

Owner     
0000000350 DNA PCR;TaqMan TNFSF4 4 Nuur Athirah Binti Mohd Daud