Variant #0001039410 (NC_000012.11:g.6443327A>C, NM_001065.3:c.123T>G (TNFRSF1A))

Chromosome 12
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.6443327A>C
DNA change (hg38) -
Published as TNFRSF1A(NM_001065.3):c.123T>G (p.D41E), TNFRSF1A(NM_001065.4):c.123T>G (p.(Asp41Glu), p.D41E)
ISCN -
DB-ID TNFRSF1A_000118 See all 4 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) 0.00017 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 2025-05-05 21:14:00 +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     
TNFRSF1A NM_001065.3 +?/. - c.123T>G r.(?) p.(Asp41Glu)


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