Variant #0000688697 (NC_000002.11:g.233388180G>T, NM_000751.2:c.-2746G>T (CHRND))

Chromosome 2
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.233388180G>T
DNA change (hg38) -
Published as PRSS56(NM_001195129.1):c.904G>T (p.V302F), PRSS56(NM_001195129.2):c.904G>T (p.(Val302Phe))
ISCN -
DB-ID CHRND_000037 See all 3 reported entries
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) 0.00106 View details
Owner VKGL-NL_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2020-09-15 15:50:26 +02:00 (CEST)
Date last edited 2025-07-08 13:22:38 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CHRND NM_000751.2 +?/. - c.-2746G>T r.(?) p.(=)
PRSS56 NM_001195129.1 +?/. - c.904G>T r.(?) p.(Val302Phe)


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