Variant #0000332936 (NC_000009.11:g.139983431G>C, NM_016219.4:c.439G>C (MAN1B1))

Chromosome 9
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.139983431G>C
DNA change (hg38) g.137088979G>C
Published as MAN1B1(NM_016219.4):c.439G>C (p.(Glu147Gln))
ISCN -
DB-ID MAN1B1_000006
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) 7.0E-5 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
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     
MAN1B1 NM_016219.4 ?/. - c.439G>C r.(?) p.(Glu147Gln)
UAP1L1 NM_207309.2 ?/. - c.*6250G>C r.(=) p.(=)


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