Variant #0001035943 (NC_000006.11:g.83884170_83884174del, NM_015599.2:c.1163_1167del (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.83884170_83884174del
DNA change (hg38) -
Published as PGM3(NM_015599.3):c.1163_1167del (p.(Lys388Ilefs*8))
ISCN -
DB-ID DOPEY1_000025
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
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.*6284_*6288del r.(=) p.(=)
PGM3 NM_015599.2 ?/. - c.1163_1167del r.(?) p.(Lys388Ilefs*8)
RWDD2A NM_033411.3 ?/. - c.-19133_-19129del r.(?) p.(=)


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