Variant #0001045495 (NC_000005.9:g.1294879G>A, NC_000005.9(NM_198253.2):c.219+7C>T (TERT))

Chromosome 5
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.1294879G>A
DNA change (hg38) -
Published as -
ISCN -
DB-ID TERT_000103 See all 5 reported entries
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs573817924
Origin Unknown
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.00032 View details
Owner MobiDetails
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by MobiDetails
Date created 2025-06-26 13:00:01 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TERT NM_198253.2 -?/. - c.219+7C>T r.(?) p.(?)


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