Variant #0001003705 (NC_000017.10:g.7454154G>A, NM_003809.2:c.322G>A (TNFSF12))

Chromosome 17
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.7454154G>A
DNA change (hg38) -
Published as TNFSF12(NM_003809.2):c.322G>A (p.(Ala108Thr)), TNFSF12(NM_003809.3):c.322G>A (p.A108T)
ISCN -
DB-ID TNFSF12_000003 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) 1.0E-5 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2024-08-28 13:16:32 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TNFSF13 NM_003808.3 ?/. - c.-8203G>A r.(?) p.(=)
TNFSF12 NM_003809.2 ?/. - c.322G>A r.(?) p.(Ala108Thr)
TNFSF12-TNFSF13 NM_172089.3 ?/. - c.322G>A r.(?) p.(Ala108Thr)


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