Variant #0000619868 (NC_000023.10:g.71813109T>C, NM_001122670.1:c.3049A>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.71813109T>C
DNA change (hg38) g.72593259T>C
Published as PHKA1(NM_002637.3):c.3088A>G (p.M1030V)
ISCN -
DB-ID PHKA1_000044
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) 2.0E-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 2019-12-04 15:24:38 +01:00 (CET)
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.3049A>G r.(?) p.(Met1017Val)
PHKA1 NM_002637.3 -?/. - c.3088A>G r.(?) p.(Met1030Val)


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