Variant #0000000155 (NC_000012.11:g.6442643C>T, NM_001065.3:c.362G>A (TNFRSF1A))

Chromosome 12
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Probably affects function
DNA change (genomic) (Relative to hg19 / GRCh37) g.6442643C>T
Reference -
DB-ID TNFRSF1A_000001
Frequency -
Average frequency (gnomAD v.2.1.1) 0.0132 View details
Owner Florian Bayersdorfer
Database submission license Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 InternationalCreative Commons License
Created by Florian Bayersdorfer
Date created 2023-06-16 11:50:15 +00:00 (UTC)
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.362G>A r.(?) p.(Arg121Gln)