Variant #0000248859 (NC_000023.10:g.153629155A>G, NM_000116.3:c.-11026A>G (TAZ))

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.153629155A>G
DNA change (hg38) g.154400814=
Published as RPL10(NM_006013.5):c.605A>G (p.N202S)
ISCN -
DB-ID RPL10_000001 See all 4 reported entries
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) 0.82294 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2023-01-11 15:44:22 +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.-11026A>G r.(?) p.(=)
DNASE1L1 NM_001009932.1 -/. - c.*1893T>C r.(=) p.(=)
RPL10 NM_006013.3 -/. - c.605A>G r.(?) p.(Asn202Ser)


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