Variant #0000808677 (NC_000019.9:g.12777468C>T, NM_000528.3:c.48G>A (MAN2B1))

Chromosome 19
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.12777468C>T
DNA change (hg38) -
Published as MAN2B1(NM_000528.3):c.48G>A (p.L16=), MAN2B1(NM_000528.4):c.48G>A (p.L16=)
ISCN -
DB-ID DHPS_000017 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) 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 2021-09-17 14:40:49 +02:00 (CEST)
Date last edited 2023-04-16 21:50:28 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MAN2B1 NM_000528.3 -?/. - c.48G>A r.(?) p.(Leu16=)
DHPS NM_001930.3 -?/. - c.*9184G>A r.(=) p.(=)
WDR83OS NM_016145.3 -?/. - c.*1705G>A r.(=) p.(=)
WDR83 NM_032332.3 -?/. - c.-3137C>T r.(?) p.(=)


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