Variant #0000655731 (NC_000007.13:g.124493082G>T, NM_015450.2:c.813C>A (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.124493082G>T
DNA change (hg38) g.124853028G>T
Published as POT1(NM_015450.2):c.813C>A (p.Y271*)
ISCN -
DB-ID POT1_000033
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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2020-03-23 16:13:27 +01:00 (CET)
Date last edited 2020-06-23 14:03:34 +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.420C>A r.(?) p.(Tyr140Ter)
POT1 NM_015450.2 +/. - c.813C>A r.(?) p.(Tyr271Ter)


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