Variant #0000619315 (NC_000023.10:g.153640231G>C, TAZ(NM_000116.3):c.51G>C)

Chromosome X
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.153640231G>C
DNA change (hg38) g.154411894G>C
Published as -
ISCN -
DB-ID RPL10_000029
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) Variant not found in online data sets
Owner VKGL-NL_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TAZ NM_000116.3 -/. - c.51G>C r.(?) p.(Trp17Cys)
DNASE1L1 NM_001009932.1 -/. - c.-434C>G r.(?) p.(=)
RPL10 NM_006013.3 -/. - c.*11036G>C r.(=) p.(=)