Variant #0000060729 (NC_000016.9:g.47727390T>A, PHKB(NM_000293.2):c.2867T>A)

Individual ID 00033818
Chromosome 16
Allele Paternal (inferred)
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.47727390T>A
DNA change (hg38) g.47693479T>A
Published as -
ISCN -
DB-ID PHKB_000004 See all 2 reported entries
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID -
Origin Germline
Segregation -
Frequency -
Re-site -
VIP 0
Methylation -
Average frequency (gnomAD v.2.1.1) Variant not found in online data sets
Owner Shu Yau
Database submission license No license selected
Created by Shu Yau
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PHKB NM_000293.2 +?/. 28 c.2867T>A r.(?) p.(Ile956Asn)



Screenings


AscendingScreening ID     

Template     

Technique     

Tissue     

Remarks     

Genes screened     

Variants found     

Owner     
0000033884 DNA SEQ;SEQ-NG-I - - PHKB 2 Shu Yau