Variant #0000329286 (NC_000003.11:g.20027099C>G, NC_000003.11(NR_027694.1):n.1292-1311G>C (PP2D1))

Chromosome 3
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.20027099C>G
DNA change (hg38) g.19985607C>G
Published as PP2D1(NM_001252657.1):c.1666G>C (p.(Glu556Gln))
ISCN -
DB-ID PP2D1_000003
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) 6.0E-5 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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-08-06 14:59:34 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
RAB5A NM_004162.4 ?/. - c.*1784C>G r.(=) p.(=)
PP2D1 NR_027694.1 ?/. - n.1292-1311G>C r.(?) -


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