Variant #0000887483 (NC_000006.11:g.83900699T>C, NM_015599.2:c.33A>G (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.83900699T>C
DNA change (hg38) -
Published as PGM3(NM_001199917.2):c.117A>G (p.A39=)
ISCN -
DB-ID DOPEY1_000018
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) 0.00095 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2022-11-01 13:01:21 +01:00 (CET)
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.*22813T>C r.(=) p.(=)
PGM3 NM_015599.2 -?/. - c.33A>G r.(?) p.(Ala11=)
RWDD2A NM_033411.3 -?/. - c.-2604T>C r.(?) p.(=)


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