Variant #0000563149 (NC_000017.10:g.7452513G>A, NM_003809.2:c.43G>A (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.7452513G>A
DNA change (hg38) g.7549196G>A
Published as TNFSF12(NM_003809.3):c.43G>A (p.E15K)
ISCN -
DB-ID TNFSF12_000001 See all 2 reported entries
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) 0.00059 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 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TNFSF13 NM_003808.3 -?/. - c.-9844G>A r.(?) p.(=)
TNFSF12 NM_003809.2 -?/. - c.43G>A r.(?) p.(Glu15Lys)
TNFSF12-TNFSF13 NM_172089.3 -?/. - c.43G>A r.(?) p.(Glu15Lys)


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