Variant #0000563152 (NC_000017.10:g.7460102C>T, NM_003809.2:c.381C>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.7460102C>T
DNA change (hg38) g.7556785C>T
Published as TNFSF12(NM_003809.3):c.381C>T (p.D127=)
ISCN -
DB-ID TNFSF12_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) 4.0E-5 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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-07-11 15:42:37 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TNFSF13 NM_003808.3 -?/. - c.-2255C>T r.(?) p.(=)
TNFSF12 NM_003809.2 -?/. - c.381C>T r.(?) p.(Asp127=)
TNFSF12-TNFSF13 NM_172089.3 -?/. - c.381C>T r.(?) p.(Asp127=)


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