Variant #0000002270 (NC_000005.10:g.95498507dupT, NM_014639.3:c.3426dupA (TTC37))

Individual ID 00000489
Chromosome 5
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg38 / GRCh38) g.95498507dupT
Published as -
Reference Way Seah Lee et al.(2016)
DB-ID TTC37_000001
dbSNP ID rs771031428
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
Date created 2021-03-08 15:30:32 +08:00 (CST)
Date last edited 2021-08-01 13:16:46 +08:00 (CST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

Published as     

RNA change     

Protein     

Clinical classification     
TTC37 NM_014639.3 +/. 33 c.3426dupA - r.(?) p.(Ala1143Serfs*4) -



Screenings


AscendingScreening ID     

Template     

Technique     

Genes screened     

Variants found     

Owner     
0000000535 DNA MCA TTC37 1 Nur Aisyah Athirah