Variant #0000947804 (NC_000002.11:g.239261463T>G, NC_000002.11(NM_015650.3):c.1452-5T>G (TRAF3IP1))

Chromosome 2
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.239261463T>G
DNA change (hg38) -
Published as TRAF3IP1(NM_001139490.1):c.1254-5T>G (p.?), TRAF3IP1(NM_015650.3):c.1452-5T>G
ISCN -
DB-ID TRAF3IP1_000016 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) 3.0E-5 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 2023-11-27 17:35:39 +01:00 (CET)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TRAF3IP1 NM_015650.3 ?/. - c.1452-5T>G r.spl? p.?


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