Variant #0000282366 (NC_000009.11:g.140002989T>C, NM_016219.4:c.2046T>C (MAN1B1))

Chromosome 9
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.140002989T>C
DNA change (hg38) g.137108537T>C
Published as MAN1B1(NM_016219.5):c.2046T>C (p.D682=)
ISCN -
DB-ID MAN1B1_000018
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) 0.76111 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2021-09-17 14:40:49 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
DPP7 NM_013379.2 -/. - c.*2111A>G r.(=) p.(=)
MAN1B1 NM_016219.4 -/. - c.2046T>C r.(?) p.(Asp682=)


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