Variant #0000951715 (NC_000023.10:g.153648381C>T, NM_000116.3:c.594C>T (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.153648381C>T
DNA change (hg38) -
Published as TAFAZZIN(NM_000116.5):c.594C>T (p.R198=), TAZ(NM_000116.5):c.594C>T (p.R198=)
ISCN -
DB-ID TAZ_000204 See all 4 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 2023-11-27 17:35:39 +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.594C>T r.(?) p.(Arg198=)
DNASE1L1 NM_001009932.1 -?/. - c.-8584G>A r.(?) p.(=)


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