Variant #0000312878 (NC_000020.10:g.57599402G>A, NM_030773.3:c.920G>A (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.57599402G>A
DNA change (hg38) g.59024347G>A
Published as TUBB1(NM_030773.4):c.920G>A (p.R307H)
ISCN -
DB-ID TUBB1_000004 See all 8 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) 0.17613 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2018-01-15 20:58:59 +01:00 (CET)
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     
ATP5E NM_006886.3 -/. - c.*4498C>T r.(=) p.(=)
SLMO2 NM_016045.2 -/. - c.*10660C>T r.(=) p.(=)
TUBB1 NM_030773.3 -/. - c.920G>A r.(?) p.(Arg307His)


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