Variant #0000316812 (NC_000017.10:g.7462934T>C, NM_003809.2:c.*2267T>C (TNFSF12))

Chromosome 17
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.7462934T>C
DNA change (hg38) g.7559617T>C
Published as TNFSF13(NM_003808.3):c.259-7T>C
ISCN -
DB-ID TNFSF12-TNFSF13_000002
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) 0.00191 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
EIF4A1 NM_001416.3 -/. - c.-13226T>C r.(?) p.(=)
TNFSF13 NM_003808.3 -/. - c.259-7T>C r.(=) p.(=)
TNFSF12 NM_003809.2 -/. - c.*2267T>C r.(=) p.(=)
SENP3 NM_015670.5 -/. - c.-2658T>C r.(?) p.(=)
TNFSF12-TNFSF13 NM_172089.3 -/. - c.499-7T>C r.(=) p.(=)


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