Variant #0001014074 (NC_000005.9:g.1294086C>T, NM_198253.2:c.915G>A (TERT))

Chromosome 5
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.1294086C>T
DNA change (hg38) -
Published as TERT(NM_198253.2):c.915G>A (p.A305=), TERT(NM_198253.3):c.915G>A (p.A305=)
ISCN -
DB-ID TERT_000097 See all 3 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) 0.28776 View details
Owner VKGL-NL_NKI
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_NKI
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     
TERT NM_198253.2 -/. - c.915G>A r.(?) p.(Ala305=)


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