Variant #0000610657 (NC_000007.13:g.124482953dup, NM_015450.2:c.1071dup (POT1))

Chromosome 7
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.124482953dup
DNA change (hg38) g.124842899dup
Published as POT1(NM_015450.3):c.1071dup (p.Gln358SerfsTer13)
ISCN -
DB-ID POT1_000031 See all 2 reported entries
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_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2019-12-04 15:24:38 +01:00 (CET)
Date last edited 2025-11-01 13:22:20 +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.678dup r.(?) p.(Gln227SerfsTer13)
POT1 NM_015450.2 ?/. - c.1071dup r.(?) p.(Gln358SerfsTer13)


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