Variant #0000856200 (NC_000022.10:g.50682590G>C, NM_020461.3:c.299C>G (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.50682590G>C
DNA change (hg38) -
Published as TUBGCP6(NM_020461.3):c.299C>G (p.P100R)
ISCN -
DB-ID HDAC10_000014
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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2022-05-09 15:47:41 +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     
TUBGCP6 NM_020461.3 ?/. - c.299C>G r.(?) p.(Pro100Arg)
HDAC10 NM_032019.5 ?/. - c.*1346C>G r.(=) p.(=)


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