Variant #0001005504 (NC_000020.10:g.57599830G>A, NM_030773.3:c.1348G>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.57599830G>A
DNA change (hg38) -
Published as TUBB1(NM_030773.3):c.1348G>A (p.(Gly450Arg))
ISCN -
DB-ID ATP5E_000016
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) 2.0E-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 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.*4070C>T r.(=) p.(=)
SLMO2 NM_016045.2 -?/. - c.*10232C>T r.(=) p.(=)
TUBB1 NM_030773.3 -?/. - c.1348G>A r.(?) p.(Gly450Arg)


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