Variant #0000526707 (NC_000006.11:g.111912649C>T, NM_001164281.2:c.641G>A (TRAF3IP2))

Chromosome 6
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.111912649C>T
DNA change (hg38) g.111591446C>T
Published as TRAF3IP2(NM_147686.4):c.641G>A (p.R214K)
ISCN -
DB-ID TRAF3IP2_000007
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) 0.00015 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 2019-07-18 18:22:55 +02:00 (CEST)
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.641G>A r.(?) p.(Arg214Lys)
TRAF3IP2-AS1 NR_034108.1 -?/. - n.486-6392C>T r.(?) -


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