Variant #0000530608 (NC_000007.13:g.124537284_124537287del, NC_000007.13(NM_015450.2):c.-39-15_-39-12del (POT1))

Chromosome 7
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.124537284_124537287del
DNA change (hg38) g.124897230_124897233del
Published as POT1(NM_015450.3):c.-39-15_-39-12delCTTT
ISCN -
DB-ID POT1_000027
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_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2021-09-17 14:40:49 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
POT1 NM_001042594.1 -?/. - c.-301-15_-301-12del r.(=) p.(=)
POT1 NM_015450.2 -?/. - c.-39-15_-39-12del r.(=) p.(=)


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