Variant #0000346469 (NC_000005.9:g.1293767G>A, NM_198253.2:c.1234C>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.1293767G>A
DNA change (hg38) g.1293652G>A
Published as TERT(NM_001193376.1):c.1234C>T (p.(His412Tyr)), TERT(NM_198253.2):c.1234C>T (p.H412Y), TERT(NM_198253.3):c.1234C>T (p.H412Y)
ISCN -
DB-ID TERT_000057 See all 10 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) 0.00325 View details
Owner VKGL-NL_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2023-07-07 10:10:56 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TERT NM_198253.2 -?/. - c.1234C>T r.(?) p.(His412Tyr)


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