Variant #0000577372 (NC_000023.10:g.71822127T>C, NC_000023.10(NM_001122670.1):c.2918-4A>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.71822127T>C
DNA change (hg38) g.72602277T>C
Published as PHKA1(NM_001122670.1):c.2918-4A>G (p.?)
ISCN -
DB-ID PHKA1_000032
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) 0.00013 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 2021-02-08 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.2918-4A>G r.spl? p.?
PHKA1 NM_002637.3 -?/. - c.2918-4A>G r.spl? p.?


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