Variant #0000572344 (NC_000022.10:g.50687601G>A, NM_020461.3:c.-4713C>T (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.50687601G>A
DNA change (hg38) g.50249172G>A
Published as HDAC10(NM_001159286.1):c.691-4C>T (p.?)
ISCN -
DB-ID HDAC10_000007
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-07-17 15:41:16 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MAPK12 NM_002969.3 -?/. - c.*4229C>T r.(=) p.(=)
TUBGCP6 NM_020461.3 -?/. - c.-4713C>T r.(?) p.(=)
HDAC10 NM_032019.5 -?/. - c.691-4C>T r.spl? p.?


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