Variant #0000613599 (NC_000011.9:g.6643810G>A, NM_000391.3:c.-3179C>T (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.6643810G>A
DNA change (hg38) g.6622579G>A
Published as DCHS1(NM_003737.4):c.9097C>T (p.R3033*)
ISCN -
DB-ID DCHS1_000230
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_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2019-12-04 15:24:38 +01:00 (CET)
Date last edited 2021-09-17 14:40:49 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TPP1 NM_000391.3 ?/. - c.-3179C>T r.(?) p.(=)
DCHS1 NM_003737.2 ?/. - c.9097C>T r.(?) p.(Arg3033*)


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