Variant #0000528489 (NC_000006.11:g.3227717C>T, NC_000006.11(NM_178012.4):c.57+4G>A (TUBB2B))

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.3227717C>T
DNA change (hg38) g.3227483C>T
Published as TUBB2B(NM_178012.4):c.57+4G>A, TUBB2B(NM_178012.5):c.57+4G>A
ISCN -
DB-ID TUBB2B_000032 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) 3.0E-5 View details
Owner VKGL-NL_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TUBB2B NM_178012.4 -?/. - c.57+4G>A r.spl? p.?


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