Variant #0000305515 (NC_000006.11:g.83878990G>A, NM_015599.2:c.1592C>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.83878990G>A
DNA change (hg38) g.83169271G>A
Published as PGM3(NM_001199917.2):c.1676C>T (p.A559V), PGM3(NM_015599.3):c.1592C>T (p.(Ala531Val))
ISCN -
DB-ID DOPEY1_000003 See all 2 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) 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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2025-05-05 21:14:00 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
DOPEY1 NM_015018.3 ?/. - c.*1104G>A r.(=) p.(=)
PGM3 NM_015599.2 ?/. - c.1592C>T r.(?) p.(Ala531Val)
RWDD2A NM_033411.3 ?/. - c.-24313G>A r.(?) p.(=)


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