Variant #0000729171 (NC_000023.10:g.71856188C>T, NM_001122670.1:c.1508G>A (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.71856188C>T
DNA change (hg38) -
Published as PHKA1(NM_002637.4):c.1508G>A (p.G503E)
ISCN -
DB-ID PHKA1_000037 See all 2 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) Retrieve
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2021-02-08 18:36:18 +01:00 (CET)
Date last edited 2023-01-11 15:44:22 +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.1508G>A r.(?) p.(Gly503Glu)
PHKA1 NM_002637.3 ?/. - c.1508G>A r.(?) p.(Gly503Glu)


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