Variant #0000867259 (NC_000023.10:g.19018032A>T, NM_000292.2:c.-15982T>A (PHKA2))

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.19018032A>T
DNA change (hg38) -
Published as ADGRG2(NM_001079858.2):c.2277T>A (p.D759E)
ISCN -
DB-ID GPR64_000035
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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2022-05-09 16:01:56 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PHKA2 NM_000292.2 ?/. - c.-15982T>A r.(?) p.(=)
GPR64 NM_001079858.2 ?/. - c.2277T>A r.(?) p.(Asp759Glu)


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