Variant #0001014276 (NC_000007.13:g.124493170T>C, NM_015450.2:c.725A>G (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.124493170T>C
DNA change (hg38) -
Published as POT1(NM_015450.2):c.725A>G (p.(Tyr242Cys))
ISCN -
DB-ID POT1_000068
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2024-10-29 21:08:56 +01:00 (CET)
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.332A>G r.(?) p.(Tyr111Cys)
POT1 NM_015450.2 ?/. - c.725A>G r.(?) p.(Tyr242Cys)


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