Variant #0000619869 (NC_000023.10:g.71813117C>G, NM_001122670.1:c.3041G>C (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.71813117C>G
DNA change (hg38) g.72593267C>G
Published as PHKA1(NM_002637.3):c.3080G>C (p.G1027A), PHKA1(NM_002637.4):c.3080G>C (p.(Gly1027Ala), p.G1027A)
ISCN -
DB-ID PHKA1_000011 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) 3.0E-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 2025-05-05 21:14:00 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PHKA1 NM_001122670.1 -?/. - c.3041G>C r.(?) p.(Gly1014Ala)
PHKA1 NM_002637.3 -?/. - c.3080G>C r.(?) p.(Gly1027Ala)


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