Variant #0000519918 (NC_000003.11:g.46751092_46751100del, NM_147196.2:c.385_393del (TMIE))

Chromosome 3
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.46751092_46751100del
DNA change (hg38) g.46709602_46709610del
Published as TMIE(NM_147196.2):c.367_375del (p.(Lys126_Lys128del))
ISCN -
DB-ID PRSS50_000004
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) Retrieve
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2019-07-18 18:22:55 +02:00 (CEST)
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     
PRSS50 NM_013270.4 -?/. - c.*2654_*2662del r.(=) p.(=)
TMIE NM_147196.2 -?/. - c.385_393del r.(?) p.(Lys129_Lys131del)


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