Variant #0000982196 (NC_000016.9:g.8895749dup, NM_000303.2:c.160dup (PMM2))

Chromosome 16
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.8895749dup
DNA change (hg38) -
Published as PMM2(NM_000303.2):c.160dupG (p.E54Gfs*6), PMM2(NM_000303.3):c.160dup (p.(Glu54Glyfs*6))
ISCN -
DB-ID PMM2_000081 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) 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 2024-04-19 20:27:30 +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     
PMM2 NM_000303.2 +/. - c.160dup r.(?) p.(Glu54GlyfsTer6)
TMEM186 NM_015421.3 +/. - c.-4277dup r.(?) p.(=)


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