Variant #0000566117 (NC_000019.9:g.12774533G>A, NM_000528.3:c.747C>T (MAN2B1))

Chromosome 19
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.12774533G>A
DNA change (hg38) g.12663719G>A
Published as MAN2B1(NM_000528.4):c.747C>T (p.T249=)
ISCN -
DB-ID DHPS_000005
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) 0.01286 View details
Owner VKGL-NL_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MAN2B1 NM_000528.3 -/. - c.747C>T r.(?) p.(Thr249=)
DHPS NM_001930.3 -/. - c.*12119C>T r.(=) p.(=)
WDR83OS NM_016145.3 -/. - c.*4640C>T r.(=) p.(=)
WDR83 NM_032332.3 -/. - c.-6072G>A r.(?) p.(=)


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