Variant #0000659209 (NC_000023.10:g.153640420del, TAZ(NM_000116.3):c.110-3del)

Chromosome X
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.153640420del
DNA change (hg38) g.154412083del
Published as TAZ(NM_001303465.1):c.165-3delC
ISCN -
DB-ID RPL10_000033
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) Variant not found in online data sets
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TAZ NM_000116.3 -?/. - c.110-3del r.spl? p.?
DNASE1L1 NM_001009932.1 -?/. - c.-622del r.(?) p.(=)
RPL10 NM_006013.3 -?/. - c.*11225del r.(?) p.(=)