Variant #0000853104 (NC_000011.9:g.6643349G>C, NM_000391.3:c.-2718C>G (TPP1))

Chromosome 11
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.6643349G>C
DNA change (hg38) -
Published as DCHS1(NM_003737.2):c.9561C>G (p.N3187K)
ISCN -
DB-ID DCHS1_000308
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) 2.0E-5 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2022-05-09 15:40:45 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TPP1 NM_000391.3 -?/. - c.-2718C>G r.(?) p.(=)
DCHS1 NM_003737.2 -?/. - c.9558C>G r.(?) p.(=)


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