Variant #0000279564 (NC_000019.9:g.12776548C>T, NM_000528.3:c.231G>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.12776548C>T
DNA change (hg38) g.12665734C>T
Published as MAN2B1(NM_000528.4):c.231G>A (p.W77*)
ISCN -
DB-ID MAN2B1_000048
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_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2018-01-15 20:58:59 +01:00 (CET)
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.231G>A r.(?) p.(Trp77Ter)
DHPS NM_001930.3 +/. - c.*10104G>A r.(=) p.(=)
WDR83OS NM_016145.3 +/. - c.*2625G>A r.(=) p.(=)
WDR83 NM_032332.3 +/. - c.-4057C>T r.(?) p.(=)


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