Variant #0000316997 (NC_000006.11:g.111912641G>T, NM_001164281.2:c.649C>A (TRAF3IP2))

Chromosome 6
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.111912641G>T
DNA change (hg38) g.111591438G>T
Published as TRAF3IP2(NM_147686.4):c.649C>A (p.P217T)
ISCN -
DB-ID TRAF3IP2_000002
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) 0.00594 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-08-06 14:59:34 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TRAF3IP2 NM_001164281.2 -/. - c.649C>A r.(?) p.(Pro217Thr)
TRAF3IP2-AS1 NR_034108.1 -/. - n.486-6400G>T r.(?) -


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