Variant #0000300746 (NC_000023.10:g.71801001T>C, NM_001122670.1:c.3484A>G (PHKA1))

Chromosome X
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification 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_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2021-09-17 14:40:49 +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.3484A>G r.(?) p.(Met1162Val)
PHKA1 NM_002637.3 -/. - c.3523A>G r.(?) p.(Met1175Val)


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