Variant #0000613587 (NC_000011.9:g.6630114G>C, NM_000391.3:c.*5663C>G (TPP1))

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.6630114G>C
DNA change (hg38) g.6608883G>C
Published as ILK(NM_004517.2):c.449-1G>C
ISCN -
DB-ID TAF10_000021
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 2019-12-04 15:24:38 +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.*5663C>G r.(=) p.(=)
ILK NM_004517.2 ?/. - c.449-1G>C r.spl? p.?
TAF10 NM_006284.3 ?/. - c.*2039C>G r.(=) p.(=)


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