Variant #0000297404 (NC_000002.11:g.233386583T>C, NM_000751.2:c.-4343T>C (CHRND))

Chromosome 2
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.233386583T>C
DNA change (hg38) g.232521873T>C
Published as PRSS56(NM_001195129.2):c.256+7T>C
ISCN -
DB-ID PRSS56_000002
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) 0.40172 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2021-09-17 14:40:49 +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.-4343T>C r.(?) p.(=)
PRSS56 NM_001195129.1 -/. - c.256+7T>C r.(=) p.(=)


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