Variant #0001035941 (NC_000006.11:g.83880202G>A, NC_000006.11(NM_015599.2):c.1366-5C>T (PGM3))

Chromosome 6
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.83880202G>A
DNA change (hg38) -
Published as PGM3(NM_001199917.2):c.1450-5C>T
ISCN -
DB-ID DOPEY1_000023
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_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2025-05-05 21:14:00 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
DOPEY1 NM_015018.3 -?/. - c.*2316G>A r.(=) p.(=)
PGM3 NM_015599.2 -?/. - c.1366-5C>T r.spl? p.?
RWDD2A NM_033411.3 -?/. - c.-23101G>A r.(?) p.(=)


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