Variant #0000002836 (NC_000022.11:g.8653C>T, TYMP(NM_001113755.3):c.972C>T)

Individual ID 00000667
Chromosome 22
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg38 / GRCh38) g.8653C>T
Published as -
Reference F L Yong et al.(2015)
DB-ID TYMP_000003 See all 2 reported entries
dbSNP ID rs131804
Frequency -
Variant remarks -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Nur Aisyah Athirah
Database submission license Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 InternationalCreative Commons License
Created by Nur Aisyah Athirah
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

Published as     

RNA change     

Protein     

Clinical classification     
TYMP NM_001113755.3 +/. 8 c.972C>T - r.(=) p.(=) Benign



Screenings


AscendingScreening ID     

Template     

Technique     

Genes screened     

Variants found     

Owner     
0000000734 DNA;RNA RT-PCR;SEQ TYMP 3 Nur Aisyah Athirah