Variant #0000530604 (NC_000007.13:g.124491972C>A, NM_015450.2:c.903G>T (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.124491972C>A
DNA change (hg38) g.124851918C>A
Published as POT1(NM_001042594.1):c.510G>T (p.(Gln170His)), POT1(NM_015450.2):c.903G>T (p.Q301H), POT1(NM_015450.3):c.903G>T (p.Q301H)
ISCN -
DB-ID POT1_000014 See all 4 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) 0.00278 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2023-11-27 17:27:23 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
POT1 NM_001042594.1 -?/. - c.510G>T r.(?) p.(Gln170His)
POT1 NM_015450.2 -?/. - c.903G>T r.(?) p.(Gln301His)


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