View genomic variant #0000000167

Individual ID 00000158
Chromosome 12
Allele Both (homozygous)
Affects function (reported) Probably affects function
Affects function (concluded) Affects function
DNA change (genomic) (Relative to hg38 / GRCh38) g.49954642G>A
Published as c.537G>A
Reference Carroll et al. (2006)
DB-ID AQP2_000012
Frequency -
Variant remarks The affected individual was homozygous; the parents were heterozygous. Variant not found in 100 control chromosomes.
Average frequency (large NGS studies) Variant not found in online data sets
Owner LOVD




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
AQP2 NM_000486.5 +?/+ 3 c.538G>A r.(?) p.(Gly180Ser)



Screenings


AscendingScreening ID     

Template     

Technique     

Genes screened     

Variants found     

Owner     
0000000159 DNA SEQ AQP2 1 LOVD