Variant #0000679278 (NC_000011.9:g.6629376A>C, NM_000391.3:c.*6401T>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.6629376A>C
DNA change (hg38) -
Published as ILK(NM_001014795.3):c.190A>C (p.N64H)
ISCN -
DB-ID ILK_000022
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_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2020-08-06 14:59:34 +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.*6401T>G r.(=) p.(=)
ILK NM_004517.2 ?/. - c.190A>C r.(?) p.(Asn64His)
TAF10 NM_006284.3 ?/. - c.*2777T>G r.(=) p.(=)
RRP8 NM_015324.3 ?/. - c.-4644T>G r.(?) p.(=)


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