Variant #0000521352 (NC_000004.11:g.119203230_119203231del, NM_003619.3:c.2488_2489del (PRSS12))

Chromosome 4
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.119203230_119203231del
DNA change (hg38) g.118282075_118282076del
Published as PRSS12(NM_003619.4):c.2488_2489delAT (p.M830Vfs*2)
ISCN -
DB-ID PRSS12_000013
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) 0.0004 View details
Owner VKGL-NL_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PRSS12 NM_003619.3 ?/. - c.2488_2489del r.(?) p.(Met830ValfsTer2)


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