Variant #0000913665 (NC_000011.9:g.6629665C>T, NM_000391.3:c.*6112G>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.6629665C>T
DNA change (hg38) -
Published as ILK(NM_004517.2):c.297C>T (p.H99=), ILK(NM_004517.4):c.297C>T (p.H99=)
ISCN -
DB-ID ILK_000004 See all 4 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) 0.26134 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2023-01-11 15:44:22 +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.*6112G>A r.(=) p.(=)
ILK NM_004517.2 -/. - c.297C>T r.(?) p.(His99=)
TAF10 NM_006284.3 -/. - c.*2488G>A r.(=) p.(=)
RRP8 NM_015324.3 -/. - c.-4933G>A r.(?) p.(=)


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