Variant #0001053795 (NC_000011.9:g.6622687C>G, NM_006284.3:c.*9466G>C (TAF10))

Chromosome 11
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.6622687C>G
DNA change (hg38) -
Published as RRP8(NM_015324.4):c.609G>C (p.(Gln203His))
ISCN -
DB-ID RRP8_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) Retrieve
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2025-11-01 13:22:20 +01:00 (CET)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TAF10 NM_006284.3 ?/. - c.*9466G>C r.(=) p.(=)
RRP8 NM_015324.3 ?/. - c.609G>C r.(?) p.(Gln203His)


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