Variant #0000861585 (NC_000009.11:g.140137399_140137406delinsCGGCCAGA, NM_006088.5:c.729_736delinsCGGCCAGA (TUBB4B))

Chromosome 9
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.140137399_140137406delinsCGGCCAGA
DNA change (hg38) -
Published as -
ISCN -
DB-ID FAM166A_000012
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_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2022-05-09 15:51:19 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
FAM166A NM_001001710.1 +?/. - c.*746_*753delinsTCTGGCCG r.(=) p.(=)
TUBB4B NM_006088.5 +?/. - c.729_736delinsCGGCCAGA r.(?) p.(Leu246Ile)


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