Variant #0000003487 (NC_000001.11:g.122511295G>T)

Individual ID 00000916
Chromosome 1
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg38 / GRCh38) g.122511295G>T
Published as -
Reference Nurul Ain Khoruddin et al. (2021), dbSNP
DB-ID chr1_000002
dbSNP ID rs4836891
Frequency -
Variant remarks -
Average frequency (gnomAD v.2.1.1) Variant not found in online data sets
Owner Noorzalifah Binti Mazuki
Database submission license Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 InternationalCreative Commons License
Created by Noorzalifah Binti Mazuki
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Variant on transcripts

Stop! No variants on transcripts found!



Screenings


AscendingScreening ID     

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Variants found     

Owner     
0000001062 DNA ? - 5 Noorzalifah Binti Mazuki