Variant #0000545073 (NC_000011.9:g.6625566A>G, NM_006284.3:c.*6587T>C (TAF10))

Chromosome 11
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.6625566A>G
DNA change (hg38) g.6604336A>G
Published as ILK(NM_001014795.2):c.65A>G (p.N22S), ILK(NM_001014795.3):c.65A>G (p.N22S)
ISCN -
DB-ID ILK_000003 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) 0.00115 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-07-18 18:22:55 +02:00 (CEST)
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.65A>G r.(?) p.(Asn22Ser)
TAF10 NM_006284.3 -?/. - c.*6587T>C r.(=) p.(=)
RRP8 NM_015324.3 -?/. - c.-834T>C r.(?) p.(=)


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