Variant #0000927816 (NC_000007.13:g.124503603G>A, NM_015450.2:c.347C>T (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.124503603G>A
DNA change (hg38) -
Published as -
ISCN -
DB-ID POT1_000005 See all 2 reported entries
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs1554426966
Origin Unknown
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner MobiDetails
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by MobiDetails
Date created 2023-06-14 19:50:01 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
POT1 NM_015450.2 ?/. - c.347C>T r.(?) p.(Pro116Leu)


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.