Variant #0000577367 (NC_000023.10:g.71801001T>C, NM_001122670.1:c.3484A>G (PHKA1))

Chromosome X
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.71801001T>C
DNA change (hg38) g.72581151T>C
Published as PHKA1(NM_001122670.1):c.3484A>G (p.(Met1162Val)), PHKA1(NM_002637.3):c.3523A>G (p.M1175V), PHKA1(NM_002637.4):c.3523A>G (p.M1175V)
ISCN -
DB-ID PHKA1_000010 See all 3 reported entries
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) 0.00155 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2021-09-17 14:40:49 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PHKA1 NM_001122670.1 -?/. - c.3484A>G r.(?) p.(Met1162Val)
PHKA1 NM_002637.3 -?/. - c.3523A>G r.(?) p.(Met1175Val)


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.