Variant #0000613580 (NC_000011.9:g.6625562G>C, NM_006284.3:c.*6591C>G (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.6625562G>C
DNA change (hg38) g.6604332G>C
Published as -
ISCN -
DB-ID RRP8_000002
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_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2019-12-04 15:24:38 +01:00 (CET)
Date last edited 2020-08-06 14:59:34 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ILK NM_004517.2 ?/. - c.61G>C r.(?) p.(Asp21His)
TAF10 NM_006284.3 ?/. - c.*6591C>G r.(=) p.(=)
RRP8 NM_015324.3 ?/. - c.-830C>G r.(?) p.(=)


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