Variant #0000319044 (NC_000006.11:g.30691495C>T, NM_178014.2:c.656C>T (TUBB))

Chromosome 6
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.30691495C>T
DNA change (hg38) g.30723718C>T
Published as TUBB(NM_178014.3):c.656C>T (p.T219I)
ISCN -
DB-ID TUBB_000003
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) Retrieve
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
FLOT1 NM_005803.2 ?/. - c.*4398G>A r.(=) p.(=)
TUBB NM_178014.2 ?/. - c.656C>T r.(?) p.(Thr219Ile)


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