Variant #0000927034 (NC_000020.10:g.57599016T>A, NM_030773.3:c.534T>A (TUBB1))

Chromosome 20
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.57599016T>A
DNA change (hg38) -
Published as TUBB1(NM_030773.3):c.534T>A (p.T178=)
ISCN -
DB-ID ATP5E_000012
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) 0.00029 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2023-04-16 21:50:28 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ATP5E NM_006886.3 -?/. - c.*4884A>T r.(=) p.(=)
SLMO2 NM_016045.2 -?/. - c.*11046A>T r.(=) p.(=)
TUBB1 NM_030773.3 -?/. - c.534T>A r.(?) p.(Thr178=)


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