Variant #0000316813 (NC_000017.10:g.7462399C>T, NM_003809.2:c.*1732C>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.7462399C>T
DNA change (hg38) g.7559082C>T
Published as TNFSF13(NM_003808.3):c.43C>T (p.P15S)
ISCN -
DB-ID TNFSF12-TNFSF13_000001
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 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)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
EIF4A1 NM_001416.3 -?/. - c.-13761C>T r.(?) p.(=)
TNFSF13 NM_003808.3 -?/. - c.43C>T r.(?) p.(Pro15Ser)
TNFSF12 NM_003809.2 -?/. - c.*1732C>T r.(=) p.(=)
SENP3 NM_015670.5 -?/. - c.-3193C>T r.(?) p.(=)
TNFSF12-TNFSF13 NM_172089.3 -?/. - c.499-542C>T r.(=) p.(=)


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