Variant #0001038627 (NC_000011.9:g.6644605G>A, NM_000391.3:c.-3974C>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.6644605G>A
DNA change (hg38) -
Published as DCHS1(NM_003737.4):c.8302C>T (p.(Arg2768Cys))
ISCN -
DB-ID DCHS1_000383
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) 0.00022 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 2025-05-05 21:14:00 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TPP1 NM_000391.3 ?/. - c.-3974C>T r.(?) p.(=)
DCHS1 NM_003737.2 ?/. - c.8302C>T r.(?) p.(Arg2768Cys)


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