Variant #0000951460 (NC_000020.10:g.57599401C>T, NM_030773.3:c.919C>T (TUBB1))

Chromosome 20
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.57599401C>T
DNA change (hg38) -
Published as TUBB1(NM_030773.3):c.919C>T (p.R307C), TUBB1(NM_030773.4):c.919C>T (p.R307C)
ISCN -
DB-ID ATP5E_000015 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) 0.0042 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 2023-11-27 17:35:39 +01:00 (CET)
Date last edited 2025-05-05 21:14:00 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ATP5E NM_006886.3 -/. - c.*4499G>A r.(=) p.(=)
SLMO2 NM_016045.2 -/. - c.*10661G>A r.(=) p.(=)
TUBB1 NM_030773.3 -/. - c.919C>T r.(?) p.(Arg307Cys)


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