Variant #0000613592 (NC_000011.9:g.6636721A>G, NM_000391.3:c.1218T>C (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.6636721A>G
DNA change (hg38) g.6615490A>G
Published as TPP1(NM_000391.3):c.1218T>C (p.Y406=)
ISCN -
DB-ID TAF10_000023
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) 4.0E-5 View details
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 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.1218T>C r.(?) p.(Tyr406=)
ILK NM_004517.2 -?/. - c.*4879A>G r.(=) p.(=)
TAF10 NM_006284.3 -?/. - c.-3301T>C r.(?) p.(=)


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