Variant #0000624516 (NC_000023.10:g.153633349G>A, NM_000116.3:c.-6832G>A (TAZ))

Chromosome X
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.153633349G>A
DNA change (hg38) g.154405008G>A
Published as DNASE1L1(NM_006730.3):c.211C>T (p.R71*)
ISCN -
DB-ID RPL10_000025
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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-12-06 12:43:26 +01:00 (CET)
Date last edited 2020-07-21 16:39:23 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TAZ NM_000116.3 ?/. - c.-6832G>A r.(?) p.(=)
DNASE1L1 NM_001009932.1 ?/. - c.211C>T r.(?) p.(Arg71Ter)
RPL10 NM_006013.3 ?/. - c.*4154G>A r.(=) p.(=)


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