Variant #0000000307 (NC_000012.11:g.102163871G>C, GNPTAB(NM_024312.4):c.1212C>G)

Individual ID 00000092
Chromosome 12
Allele Both (homozygous)
Affects function (as reported) Affects function
Affects function (by curator) Affects function
DNA change (genomic) (Relative to hg19 / GRCh37) g.102163871G>C
Reference -
DB-ID GNPTAB_000001
Average frequency (gnomAD v.2.1.1) Variant not found in online data sets
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     

Clinical classification     
GNPTAB NM_024312.4 +/+ - c.1212C>G r.(?) p.(Tyr404*) pathogenic



Screenings


AscendingScreening ID     

Template     

Technique     

Genes screened     

Variants found     

Owner     
0000000095 DNA SEQ-NG GNPTAB 1 Variome.ir