Variant #0000849808 (NC_000002.11:g.239237846G>A, NM_015650.3:c.778G>A (TRAF3IP1))

Chromosome 2
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.239237846G>A
DNA change (hg38) -
Published as TRAF3IP1(NM_015650.3):c.778G>A (p.E260K), TRAF3IP1(NM_015650.4):c.778G>A (p.E260K)
ISCN -
DB-ID TRAF3IP1_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) 0.00532 View details
Owner VKGL-NL_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2022-05-09 15:40:45 +02:00 (CEST)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TRAF3IP1 NM_015650.3 -/. - c.778G>A r.(?) p.(Glu260Lys)


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