Variant #0000806252 (NC_000014.8:g.103369730G>A, NM_145725.2:c.1099G>A (TRAF3))

Chromosome 14
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.103369730G>A
DNA change (hg38) -
Published as TRAF3(NM_003300.4):c.1099G>A (p.V367M), TRAF3(NM_145725.2):c.1099G>A (p.V367M), TRAF3(NM_145725.3):c.1099G>A (p.(Val367Met))
ISCN -
DB-ID TRAF3_000018 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) 8.0E-5 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2021-09-17 14:40:49 +02:00 (CEST)
Date last edited 2025-05-05 21:14:00 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TRAF3 NM_145725.2 ?/. - c.1099G>A r.(?) p.(Val367Met)


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