Variant #0000000059 (NC_000023.10:g.18665333G>C, RS1(NM_000330.3):c.304C>G)

Individual ID 00000080
Chromosome X
Allele Maternal (inferred)
Affects function (as reported) Affects function
Affects function (by curator) Affects function
DNA change (genomic) (Relative to hg19 / GRCh37) g.18665333G>C
Reference -
DB-ID RS1_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
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

Classification     
RS1 NM_000330.3 +/+ - c.304C>G r.(?) p.(Arg102Gly) Likely Pathogenic



Screenings


AscendingScreening ID     

Template     

Technique     

Genes screened     

Variants found     

Owner     
0000000081 DNA SEQ-NG RS1 1 variome.ir