Variant #0000000026 (NC_000007.13:g.128041131T>C, IMPDH1(NM_001142574.1):c.187A>G)

Individual ID 00000032
Chromosome 7
Allele Parent #1
Affects function (as reported) Effect unknown
Affects function (by curator) Effect unknown
DNA change (genomic) (Relative to hg19 / GRCh37) g.128041131T>C
Reference -
DB-ID IMPDH1_000001
Average frequency (gnomAD v.2.1.1) Retrieve
Owner variome.ir
Database submission license Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 InternationalCreative Commons License
Created by variome.ir
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

Classification     
IMPDH1 NM_001142574.1 ?/? - c.187A>G r.(?) p.(Thr63Ala) VUS



Screenings


AscendingScreening ID     

Template     

Technique     

Genes screened     

Variants found     

Owner     
0000000033 DNA SEQ-NG IMPDH1 1 variome.ir