Variant #0001037366 (NC_000009.11:g.140002982G>C, NM_016219.4:c.2039G>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.140002982G>C
DNA change (hg38) -
Published as MAN1B1(NM_016219.5):c.2039G>C (p.(Ser680Thr))
ISCN -
DB-ID DPP7_000019
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) 0.00011 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 2025-05-05 21:14:00 +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     
DPP7 NM_013379.2 ?/. - c.*2118C>G r.(=) p.(=)
MAN1B1 NM_016219.4 ?/. - c.2039G>C r.(?) p.(Ser680Thr)


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