Variant #0000574833 (NC_000023.10:g.153627842A>G, NM_000116.3:c.-12339A>G (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.153627842A>G
DNA change (hg38) g.154399501A>G
Published as RPL10(NM_001303625.1):c.97A>G (p.I33V)
ISCN -
DB-ID RPL10_000013
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 2019-07-18 18:22:55 +02:00 (CEST)
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.-12339A>G r.(?) p.(=)
DNASE1L1 NM_001009932.1 ?/. - c.*3206T>C r.(=) p.(=)
RPL10 NM_006013.3 ?/. - c.97A>G r.(?) p.(Ile33Val)


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