Variant #0000681032 (NC_000017.10:g.7453463C>T, NM_003809.2:c.234C>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.7453463C>T
DNA change (hg38) -
Published as TNFSF12(NM_003809.3):c.234C>T (p.S78=)
ISCN -
DB-ID TNFSF12_000005
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_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2020-08-06 14:59:34 +02:00 (CEST)
Date last edited 2021-09-17 14:40:49 +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.-8894C>T r.(?) p.(=)
TNFSF12 NM_003809.2 -?/. - c.234C>T r.(?) p.(Ser78=)
TNFSF12-TNFSF13 NM_172089.3 -?/. - c.234C>T r.(?) p.(Ser78=)


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