Variant #0000529932 (NC_000006.11:g.83889684T>G, NM_015599.2:c.790A>C (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.83889684T>G
DNA change (hg38) g.83179965T>G
Published as PGM3(NM_001199917.2):c.874A>C (p.M292L)
ISCN -
DB-ID DOPEY1_000008
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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
DOPEY1 NM_015018.3 -?/. - c.*11798T>G r.(=) p.(=)
PGM3 NM_015599.2 -?/. - c.790A>C r.(?) p.(Met264Leu)
RWDD2A NM_033411.3 -?/. - c.-13619T>G r.(?) p.(=)


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