Variant #0000915653 (NC_000023.10:g.153649179_153649191del, NC_000023.10(NM_000116.3):c.778-63_778-51del (TAZ))

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.153649179_153649191del
DNA change (hg38) -
Published as TAZ(NM_000116.5):c.778-80_778-68delCACCCTCCCAGGG
ISCN -
DB-ID TAZ_000194 See all 2 reported entries
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_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2023-01-11 15:44:22 +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     
TAZ NM_000116.3 -?/. - c.778-63_778-51del r.(=) p.(=)
DNASE1L1 NM_001009932.1 -?/. - c.-9377_-9365del r.(?) p.(=)


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