Variant #0000000025 (NC_000011.9:g.61730302C>T, BEST1(NM_004183.3):c.1676C>T)

Individual ID 00000031
Chromosome 11
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.61730302C>T
Reference -
DB-ID BEST1_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     
BEST1 NM_004183.3 +?/+? - c.1676C>T r.(?) p.(Ser559Leu) VUS LP



Screenings


AscendingScreening ID     

Template     

Technique     

Genes screened     

Variants found     

Owner     
0000000032 DNA SEQ-NG BEST1 1 variome.ir