Variant #0000805294 (NC_000011.9:g.6636232T>C, NC_000011.9(NM_000391.3):c.1426-10A>G (TPP1))

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.6636232T>C
DNA change (hg38) -
Published as TPP1(NM_000391.3):c.1426-10A>G
ISCN -
DB-ID ILK_000030
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) 0.00011 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 2021-09-17 14:40:49 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TPP1 NM_000391.3 -?/. - c.1426-10A>G r.(=) p.(=)
ILK NM_004517.2 -?/. - c.*4390T>C r.(=) p.(=)
TAF10 NM_006284.3 -?/. - c.-2812A>G r.(?) p.(=)


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