Variant #0000728218 (NC_000022.10:g.50682847G>T, NM_020461.3:c.42C>A (TUBGCP6))

Chromosome 22
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.50682847G>T
DNA change (hg38) -
Published as TUBGCP6(NM_020461.3):c.42C>A (p.A14=)
ISCN -
DB-ID HDAC10_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) 0.00098 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2021-02-08 18:36:18 +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.42C>A r.(?) p.(Ala14=)
HDAC10 NM_032019.5 -?/. - c.*1089C>A r.(=) p.(=)


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