Variant #0000336226 (NC_000023.10:g.153633161G>C, NM_000116.3:c.-7020G>C (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.153633161G>C
DNA change (hg38) g.154404820G>C
Published as DNASE1L1(NM_001009932.1):c.311+8C>G (p.(=))
ISCN -
DB-ID DNASE1L1_000024
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) 5.0E-5 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TAZ NM_000116.3 ?/. - c.-7020G>C r.(?) p.(=)
DNASE1L1 NM_001009932.1 ?/. - c.311+8C>G r.(=) p.(=)
RPL10 NM_006013.3 ?/. - c.*3966G>C r.(=) p.(=)


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