Variant #0000914977 (NC_000017.10:g.7462469C>T, NM_003809.2:c.*1802C>T (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.7462469C>T
DNA change (hg38) -
Published as TNFSF13(NM_003808.3):c.113C>T (p.A38V)
ISCN -
DB-ID EIF4A1_000008
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) 0.00024 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2023-01-11 15:44:22 +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.-13691C>T r.(?) p.(=)
TNFSF13 NM_003808.3 -?/. - c.113C>T r.(?) p.(Ala38Val)
TNFSF12 NM_003809.2 -?/. - c.*1802C>T r.(=) p.(=)
SENP3 NM_015670.5 -?/. - c.-3123C>T r.(?) p.(=)
TNFSF12-TNFSF13 NM_172089.3 -?/. - c.499-472C>T r.(=) p.(=)


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