Variant #0000994639 (NC_000005.9:g.1293863G>A, NM_198253.2:c.1138C>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.1293863G>A
DNA change (hg38) -
Published as TERT(NM_198253.2):c.1138C>T (p.P380S), TERT(NM_198253.3):c.1138C>T (p.P380S)
ISCN -
DB-ID TERT_000096 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) 0.00076 View details
Owner VKGL-NL_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2024-08-28 13:16:32 +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.1138C>T r.(?) p.(Pro380Ser)


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