Variant #0000861584 (NC_000009.11:g.140136235C>T, NM_006088.5:c.120C>T (TUBB4B))

Chromosome 9
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.140136235C>T
DNA change (hg38) -
Published as TUBB4B(NM_006088.6):c.120C>T (p.S40=)
ISCN -
DB-ID FAM166A_000011
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 2022-05-09 15:51:19 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
FAM166A NM_001001710.1 -?/. - c.*1917G>A r.(=) p.(=)
TUBB4B NM_006088.5 -?/. - c.120C>T r.(?) p.(Ser40=)


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