Variant #0001006096 (NC_000022.10:g.40662881A>G, NM_001162501.1:c.2647A>G (TNRC6B))

Chromosome 22
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.40662881A>G
DNA change (hg38) -
Published as TNRC6B(NM_001162501.1):c.2647A>G (p.(Ile883Val)), TNRC6B(NM_001162501.2):c.2647A>G (p.I883V)
ISCN -
DB-ID TNRC6B_000051 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 2024-08-28 13:16:32 +02:00 (CEST)
Date last edited 2024-10-29 21:08:56 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TNRC6B NM_001162501.1 -?/. - c.2647A>G r.(?) p.(Ile883Val)


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