Variant #0000537535 (NC_000009.11:g.140002923C>T, NM_016219.4:c.1980C>T (MAN1B1))

Chromosome 9
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.140002923C>T
DNA change (hg38) g.137108471C>T
Published as MAN1B1(NM_016219.4):c.1980C>T (p.F660=)
ISCN -
DB-ID DPP7_000010
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) 0.00214 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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-06-26 13:00:47 +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.*2177G>A r.(=) p.(=)
MAN1B1 NM_016219.4 -?/. - c.1980C>T r.(?) p.(Phe660=)


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