Variant #0000915413 (NC_000020.10:g.57599527G>A, NM_030773.3:c.1045G>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.57599527G>A
DNA change (hg38) -
Published as TUBB1(NM_030773.3):c.1045G>A (p.V349I), TUBB1(NM_030773.4):c.1045G>A (p.V349I)
ISCN -
DB-ID ATP5E_000011 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) 0.00174 View details
Owner VKGL-NL_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2023-01-11 15:44:22 +01:00 (CET)
Date last edited 2023-11-27 17:27:23 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ATP5E NM_006886.3 -?/. - c.*4373C>T r.(=) p.(=)
SLMO2 NM_016045.2 -?/. - c.*10535C>T r.(=) p.(=)
TUBB1 NM_030773.3 -?/. - c.1045G>A r.(?) p.(Val349Ile)


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