Variant #0000983318 (NC_000019.9:g.18260214C>T, NM_005027.3:c.-4314C>T (PIK3R2))

Chromosome 19
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.18260214C>T
DNA change (hg38) -
Published as MAST3(NM_015016.2):c.3608C>T (p.(Ser1203Leu))
ISCN -
DB-ID MAST3_000016
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2024-04-19 20:27:30 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PIK3R2 NM_005027.3 ?/. - c.-4314C>T r.(?) p.(=)
MAST3 NM_015016.1 ?/. - c.3608C>T r.(?) p.(Ser1203Leu)


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