Variant #0000000063 (NC_000007.13:g.128038574T>C, IMPDH1(NM_001142574.1):c.698A>G)

Individual ID 00000084
Chromosome 7
Allele Parent #1
Affects function (as reported) Probably affects function
Affects function (by curator) Probably affects function
DNA change (genomic) (Relative to hg19 / GRCh37) g.128038574T>C
Reference -
DB-ID IMPDH1_000002
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
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

Classification     
IMPDH1 NM_001142574.1 +?/+? - c.698A>G r.(?) p.(Lys233Arg) VUS LP



Screenings


AscendingScreening ID     

Template     

Technique     

Genes screened     

Variants found     

Owner     
0000000085 DNA SEQ-NG IMPDH1 1 variome.ir