Variant #0000967039 (NC_000012.11:g.6442643C>G, NM_001065.3:c.362G>C (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.6442643C>G
DNA change (hg38) -
Published as TNFRSF1A(NM_001065.3):c.362G>C (p.R121P)
ISCN -
DB-ID PLEKHG6_000012 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 View details
Owner VKGL-NL_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2024-02-26 20:06:56 +01:00 (CET)
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>C r.(?) p.(Arg121Pro)
PLEKHG6 NM_018173.3 +?/. - c.*5332C>G r.(=) p.(=)


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