Variant #0000530600 (NC_000007.13:g.124469393_124469396del, NM_015450.2:c.1507_1510del (POT1))

Chromosome 7
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.124469393_124469396del
DNA change (hg38) g.124829339_124829342del
Published as POT1(NM_015450.3):c.1507_1510delTGTA (p.C503Nfs*6)
ISCN -
DB-ID POT1_000022
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_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
POT1 NM_001042594.1 +/. - c.1114_1117del r.(?) p.(Cys372AsnfsTer6)
POT1 NM_015450.2 +/. - c.1507_1510del r.(?) p.(Cys503AsnfsTer6)


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