Variant #0000677896 (NC_000006.11:g.83889675T>G, NM_015599.2:c.799A>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.83889675T>G
DNA change (hg38) -
Published as PGM3(NM_001199917.2):c.883A>C (p.K295Q), PGM3(NM_001367287.1):c.883A>C (p.K295Q)
ISCN -
DB-ID DOPEY1_000012 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) 0 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2020-08-06 14:59:34 +02:00 (CEST)
Date last edited 2022-11-01 13:01:21 +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.*11789T>G r.(=) p.(=)
PGM3 NM_015599.2 -?/. - c.799A>C r.(?) p.(Lys267Gln)
RWDD2A NM_033411.3 -?/. - c.-13628T>G r.(?) p.(=)


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