Variant #0000000020 (NC_000002.11:g.73679503_73679504delTC, ALMS1(NM_015120.4):c.5846_5847delTC)

Individual ID 00000022
Chromosome 2
Allele Both (homozygous)
Affects function (as reported) Affects function
Affects function (by curator) Affects function
DNA change (genomic) (Relative to hg19 / GRCh37) g.73679503_73679504delTC
Reference -
DB-ID ALMS1_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     
ALMS1 NM_015120.4 +/+ - c.5846_5847delTC r.(?) p.(Gln1951Thrfs*34) Likely Pathogenic



Screenings


AscendingScreening ID     

Template     

Technique     

Genes screened     

Variants found     

Owner     
0000000023 DNA SEQ-NG ALMS1 1 variome.ir