Variant #0000693728 (NC_000023.10:g.71846869A>G, NM_001122670.1:c.1745T>C (PHKA1))

Chromosome X
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.71846869A>G
DNA change (hg38) -
Published as PHKA1(NM_002637.3):c.1745T>C (p.I582T)
ISCN -
DB-ID PHKA1_000052
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 1.0E-5 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2020-09-15 15:50:26 +02:00 (CEST)
Date last edited 2021-02-08 18:36:18 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PHKA1 NM_001122670.1 ?/. - c.1745T>C r.(?) p.(Ile582Thr)
PHKA1 NM_002637.3 ?/. - c.1745T>C r.(?) p.(Ile582Thr)


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