Variant #0000802890 (NC_000007.13:g.124499002_124499003delinsCA, NC_000007.13(NM_015450.2):c.702+8_702+9delinsTG (POT1))

Chromosome 7
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.124499002_124499003delinsCA
DNA change (hg38) -
Published as POT1(NM_015450.3):c.702+8_702+9delATinsTG
ISCN -
DB-ID POT1_000040
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_NKI
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_NKI
Date created 2021-09-17 14:40:49 +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     
POT1 NM_001042594.1 -/. - c.309+8_309+9delinsTG r.(=) p.(=)
POT1 NM_015450.2 -/. - c.702+8_702+9delinsTG r.(=) p.(=)


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