Variant #0000291424 (NC_000019.9:g.12776226G>A, NM_000528.3:c.376C>T (MAN2B1))

Chromosome 19
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.12776226G>A
DNA change (hg38) g.12665412G>A
Published as MAN2B1(NM_000528.3):c.376C>T (p.R126C)
ISCN -
DB-ID MAN2B1_000046
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) 2.0E-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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-03-23 16:13:27 +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.376C>T r.(?) p.(Arg126Cys)
DHPS NM_001930.3 ?/. - c.*10426C>T r.(=) p.(=)
WDR83OS NM_016145.3 ?/. - c.*2947C>T r.(=) p.(=)
WDR83 NM_032332.3 ?/. - c.-4379G>A r.(?) p.(=)


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