Variant #0000336222 (NC_000023.10:g.153629183C>T, NM_000116.3:c.-10998C>T (TAZ))

Chromosome X
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.153629183C>T
DNA change (hg38) g.154400842C>T
Published as RPL10(NM_001256577.1):c.470C>T (p.(Pro157Leu))
ISCN -
DB-ID RPL10_000006
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) 0.00181 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 2020-07-21 16:35:31 +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.-10998C>T r.(?) p.(=)
DNASE1L1 NM_001009932.1 -?/. - c.*1865G>A r.(=) p.(=)
RPL10 NM_006013.3 -?/. - c.633C>T r.(?) p.(Ala211=)


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