Variant #0000622688 (NC_000011.9:g.6640422C>G, NC_000011.9(NM_000391.3):c.89+5G>C (TPP1))

Chromosome 11
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.6640422C>G
DNA change (hg38) g.6619191C>G
Published as TPP1(NM_000391.4):c.89+5G>C
ISCN -
DB-ID TPP1_000014 See all 9 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 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 2019-12-06 12:43:26 +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.89+5G>C r.spl? p.?
DCHS1 NM_003737.2 +?/. - c.*2588G>C r.(=) p.(=)


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