Variant #0001057230 (NC_000022.10:g.50662846C>T, NM_020461.3:c.2069G>A (TUBGCP6))

Chromosome 22
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.50662846C>T
DNA change (hg38) -
Published as TUBGCP6(NM_020461.4):c.2069G>A (p.(Arg690Gln))
ISCN -
DB-ID TUBGCP6_000143
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 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     
TUBGCP6 NM_020461.3 ?/. - c.2069G>A r.(?) p.(Arg690Gln)


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