Variant #0000545132 (NC_000011.9:g.6630943G>A, NM_000391.3:c.*4834C>T (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.6630943G>A
DNA change (hg38) g.6609712G>A
Published as ILK(NM_001014795.3):c.857-12G>A
ISCN -
DB-ID TAF10_000008
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) 0.00042 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
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     
TPP1 NM_000391.3 -/. - c.*4834C>T r.(=) p.(=)
ILK NM_004517.2 -/. - c.857-12G>A r.(=) p.(=)
TAF10 NM_006284.3 -/. - c.*1210C>T r.(=) p.(=)


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