Variant #0000727128 (NC_000019.9:g.12777451C>T, NM_000528.3:c.65G>A (MAN2B1))

Chromosome 19
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.12777451C>T
DNA change (hg38) -
Published as MAN2B1(NM_000528.3):c.65G>A (p.W22*)
ISCN -
DB-ID DHPS_000012
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) 1.0E-5 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 2021-02-08 18:36:18 +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     
MAN2B1 NM_000528.3 +/. - c.65G>A r.(?) p.(Trp22*)
DHPS NM_001930.3 +/. - c.*9201G>A r.(=) p.(=)
WDR83OS NM_016145.3 +/. - c.*1722G>A r.(=) p.(=)
WDR83 NM_032332.3 +/. - c.-3154C>T r.(?) p.(=)


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