Variant #0000894293 (NC_000017.10:g.7463352_7463353del, NM_003809.2:c.*2685_*2686del (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.7463352_7463353del
DNA change (hg38) -
Published as TNFSF13(NM_003808.3):c.386-14_386-13delAC
ISCN -
DB-ID EIF4A1_000007
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_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2022-11-01 13:41:49 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
EIF4A1 NM_001416.3 -?/. - c.-12808_-12807del r.(?) p.(=)
TNFSF13 NM_003808.3 -?/. - c.386-14_386-13del r.(=) p.(=)
TNFSF12 NM_003809.2 -?/. - c.*2685_*2686del r.(=) p.(=)
SENP3 NM_015670.5 -?/. - c.-2240_-2239del r.(?) p.(=)
TNFSF12-TNFSF13 NM_172089.3 -?/. - c.626-14_626-13del r.(=) p.(=)


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