Variant #0000331105 (NC_000006.11:g.83900538T>A, NM_015599.2:c.194A>T (PGM3))

Chromosome 6
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.83900538T>A
DNA change (hg38) g.83190819T>A
Published as PGM3(NM_001199917.1):c.278A>T (p.(His93Leu))
ISCN -
DB-ID PGM3_000002
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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-08-06 14:59:34 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
DOPEY1 NM_015018.3 ?/. - c.*22652T>A r.(=) p.(=)
PGM3 NM_015599.2 ?/. - c.194A>T r.(?) p.(His65Leu)
RWDD2A NM_033411.3 ?/. - c.-2765T>A r.(?) p.(=)


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.