Variant #0000289608 (NC_000011.9:g.6630109C>T, NM_000391.3:c.*5668G>A (TPP1))

Chromosome 11
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.6630109C>T
DNA change (hg38) g.6608878C>T
Published as ILK(NM_004517.2):c.449-6C>T
ISCN -
DB-ID ILK_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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-08-06 14:59:34 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TPP1 NM_000391.3 -/. - c.*5668G>A r.(=) p.(=)
ILK NM_004517.2 -/. - c.449-6C>T r.(=) p.(=)
TAF10 NM_006284.3 -/. - c.*2044G>A r.(=) p.(=)


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