Variant #0000987855 (NC_000016.9:g.30762443G>A, NM_000294.2:c.112G>A (PHKG2))

Chromosome 16
Allele Unknown
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.30762443G>A
DNA change (hg38) -
Published as -
ISCN -
DB-ID PHKG2_000020
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs1353903670
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0 View details
Owner MobiDetails
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by MobiDetails
Date created 2024-06-27 16:23:01 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PHKG2 NM_000294.2 +?/. - c.112G>A r.(?) p.(Val38Ile)


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