Variant #0000858407 (NC_000002.11:g.233387234T>G, NM_000751.2:c.-3692T>G (CHRND))

Chromosome 2
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.233387234T>G
DNA change (hg38) -
Published as PRSS56(NM_001195129.1):c.456T>G (p.N152K)
ISCN -
DB-ID CHRND_000066
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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2022-05-09 15:51:19 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CHRND NM_000751.2 ?/. - c.-3692T>G r.(?) p.(=)
PRSS56 NM_001195129.1 ?/. - c.456T>G r.(?) p.(Asn152Lys)


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