Variant #0000931461 (NC_000023.10:g.71872498C>T, NM_001122670.1:c.1141G>A (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.71872498C>T
DNA change (hg38) -
Published as PHKA1(NM_001122670.1):c.1141G>A (p.(Asp381Asn)), PHKA1(NM_002637.3):c.1141G>A (p.D381N), PHKA1(NM_002637.4):c.1141G>A (p.D381N)
ISCN -
DB-ID PHKA1_000021 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) 0.00055 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2023-07-07 10:10:56 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PHKA1 NM_001122670.1 -?/. - c.1141G>A r.(?) p.(Asp381Asn)
PHKA1 NM_002637.3 -?/. - c.1141G>A r.(?) p.(Asp381Asn)


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