Variant #0000622683 (NC_000011.9:g.6625579C>A, NM_006284.3:c.*6574G>T (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.6625579C>A
DNA change (hg38) g.6604349C>A
Published as ILK(NM_001014795.3):c.78C>A (p.D26E)
ISCN -
DB-ID RRP8_000003
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_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2019-12-06 12:43:26 +01:00 (CET)
Date last edited 2021-09-17 14:40:49 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ILK NM_004517.2 ?/. - c.78C>A r.(?) p.(Asp26Glu)
TAF10 NM_006284.3 ?/. - c.*6574G>T r.(=) p.(=)
RRP8 NM_015324.3 ?/. - c.-847G>T r.(?) p.(=)


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