Variant #0000930999 (NC_000019.9:g.12776514C>G, NC_000019.9(NM_000528.3):c.262+3G>C (MAN2B1))

Chromosome 19
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.12776514C>G
DNA change (hg38) -
Published as MAN2B1(NM_000528.4):c.262+3G>C
ISCN -
DB-ID DHPS_000024
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_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2023-07-07 10:10:56 +02:00 (CEST)
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.262+3G>C r.spl? p.?
DHPS NM_001930.3 +?/. - c.*10138G>C r.(=) p.(=)
WDR83OS NM_016145.3 +?/. - c.*2659G>C r.(=) p.(=)
WDR83 NM_032332.3 +?/. - c.-4091C>G r.(?) p.(=)


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