Variant #0000336225 (NC_000023.10:g.153631291C>T, NM_000116.3:c.-8890C>T (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.153631291C>T
DNA change (hg38) g.154402950C>T
Published as DNASE1L1(NM_001009932.1):c.766G>A (p.(Glu256Lys))
ISCN -
DB-ID DNASE1L1_000023
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) 1.0E-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.-8890C>T r.(?) p.(=)
DNASE1L1 NM_001009932.1 ?/. - c.766G>A r.(?) p.(Glu256Lys)
RPL10 NM_006013.3 ?/. - c.*2096C>T r.(=) p.(=)


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