Variant #0000545167 (NC_000011.9:g.6638271G>A, NM_000391.3:c.622C>T (TPP1))

Chromosome 11
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.6638271G>A
DNA change (hg38) g.6617040G>A
Published as TPP1(NM_000391.3):c.622C>T (p.R208*, p.(Arg208Ter)), TPP1(NM_000391.4):c.622C>T (p.R208*)
ISCN -
DB-ID TPP1_000043 See all 175 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) 0.00024 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2019-07-18 18:22:55 +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.622C>T r.(?) p.(Arg208Ter)
DCHS1 NM_003737.2 +/. - c.*4739C>T r.(=) p.(=)
TAF10 NM_006284.3 +/. - c.-4851C>T r.(?) p.(=)


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