Variant #0000563153 (NC_000017.10:g.7466648_7466650del, NM_003809.2:c.*5981_*5983del (TNFSF12))

Chromosome 17
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.7466648_7466650del
DNA change (hg38) g.7563331_7563333del
Published as SENP3(NM_015670.5):c.241_243del (p.(Glu81del))
ISCN -
DB-ID EIF4A1_000004
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-08-06 14:59:34 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
EIF4A1 NM_001416.3 -?/. - c.-9512_-9510del r.(?) p.(=)
TNFSF13 NM_003808.3 -?/. - c.*2498_*2500del r.(=) p.(=)
TNFSF12 NM_003809.2 -?/. - c.*5981_*5983del r.(=) p.(=)
SENP3 NM_015670.5 -?/. - c.255_257del r.(?) p.(Glu85del)
TNFSF12-TNFSF13 NM_172089.3 -?/. - c.*2498_*2500del r.(=) p.(=)
SENP3-EIF4A1 NR_037926.1 -?/. - n.538_540del r.(?) -


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