Variant #0000723607 (NC_000011.9:g.6629650T>C, NM_000391.3:c.*6127A>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.6629650T>C
DNA change (hg38) -
Published as ILK(NM_004517.2):c.282T>C (p.N94=)
ISCN -
DB-ID ILK_000027
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) 0.00017 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2021-02-08 18:36:18 +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.*6127A>G r.(=) p.(=)
ILK NM_004517.2 -?/. - c.282T>C r.(?) p.(Asn94=)
TAF10 NM_006284.3 -?/. - c.*2503A>G r.(=) p.(=)
RRP8 NM_015324.3 -?/. - c.-4918A>G r.(?) p.(=)


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