Variant #0001053473 (NC_000009.11:g.140145754C>T, NM_006088.5:c.*7746C>T (TUBB4B))

Chromosome 9
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.140145754C>T
DNA change (hg38) -
Published as STPG3(NM_001004353.3):c.16C>T (p.(Gln6*))
ISCN -
DB-ID C9orf173_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) 2.0E-5 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2025-11-01 13:22:20 +01:00 (CET)
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.-3587G>A r.(?) p.(=)
C9orf173 NM_001004353.3 ?/. - c.16C>T r.(?) p.(Gln6*)
TUBB4B NM_006088.5 ?/. - c.*7746C>T r.(=) p.(=)
NELFB NM_015456.3 ?/. - c.-4208C>T r.(?) p.(=)


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