Variant #0000332942 (NC_000009.11:g.140006378G>A, NM_016219.4:c.*3335G>A (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.140006378G>A
DNA change (hg38) g.137111926G>A
Published as DPP7(NM_013379.2):c.1154C>T (p.(Thr385Ile))
ISCN -
DB-ID DPP7_000001
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) 0.00532 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     
DPP7 NM_013379.2 -?/. - c.1154C>T r.(?) p.(Thr385Ile)
MAN1B1 NM_016219.4 -?/. - c.*3335G>A r.(=) p.(=)


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