Variant #0000313271 (NC_000005.9:g.1294397C>T, NM_198253.2:c.604G>A (TERT))

Chromosome 5
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.1294397C>T
DNA change (hg38) g.1294282C>T
Published as TERT(NM_001193376.1):c.604G>A (p.(Ala202Thr)), TERT(NM_198253.2):c.604G>A (p.A202T), TERT(NM_198253.3):c.604G>A (p.A202T)
ISCN -
DB-ID TERT_000003 See all 5 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) 0.0003 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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TERT NM_198253.2 ?/. - c.604G>A r.(?) p.(Ala202Thr)


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