Variant #0001026052 (NC_000011.9:g.6629353G>T, NM_000391.3:c.*6424C>A (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.6629353G>T
DNA change (hg38) -
Published as ILK(NM_001014795.3):c.167G>T (p.R56L)
ISCN -
DB-ID RRP8_000004 See all 2 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) Retrieve
Owner VKGL-NL_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2025-02-07 18:57:27 +01:00 (CET)
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.*6424C>A r.(=) p.(=)
ILK NM_004517.2 ?/. - c.167G>T r.(?) p.(Arg56Leu)
TAF10 NM_006284.3 ?/. - c.*2800C>A r.(=) p.(=)
RRP8 NM_015324.3 ?/. - c.-4621C>A r.(?) p.(=)


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