Variant #0000526705 (NC_000006.11:g.111896863T>C, NM_001164281.2:c.1184A>G (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.111896863T>C
DNA change (hg38) g.111575660T>C
Published as TRAF3IP2(NM_147686.4):c.1184A>G (p.N395S)
ISCN -
DB-ID TRAF3IP2_000006 See all 3 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) 0.00216 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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2023-04-16 21:50:28 +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.1184A>G r.(?) p.(Asn395Ser)
TRAF3IP2-AS1 NR_034108.1 -?/. - n.377-702T>C r.(?) -


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