Variant #0000545163 (NC_000011.9:g.6637756_6637759del, NC_000011.9(NM_000391.3):c.887-9_887-6del (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.6637756_6637759del
DNA change (hg38) g.6616525_6616528del
Published as TPP1(NM_000391.3):c.887-9_887-6del (p.(=))
ISCN -
DB-ID DCHS1_000118
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_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 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TPP1 NM_000391.3 ?/. - c.887-9_887-6del r.(=) p.(=)
DCHS1 NM_003737.2 ?/. - c.*5267_*5270del r.(=) p.(=)
TAF10 NM_006284.3 ?/. - c.-4323_-4320del r.(?) p.(=)


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