Variant #0000887059 (NC_000006.11:g.138200216C>T, NM_006290.3:c.1634C>T (TNFAIP3))

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.138200216C>T
DNA change (hg38) -
Published as TNFAIP3(NM_001270508.2):c.1634C>T (p.A545V), TNFAIP3(NM_006290.4):c.1634C>T (p.A545V)
ISCN -
DB-ID TNFAIP3_000012 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) 0.00044 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 2022-11-01 13:01:21 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TNFAIP3 NM_006290.3 -?/. - c.1634C>T r.(?) p.(Ala545Val)


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