Variant #0001051134 (NC_000002.11:g.233390936C>T, NM_000751.2:c.11C>T (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.233390936C>T
DNA change (hg38) -
Published as CHRND(NM_000751.3):c.11C>T (p.(Pro4Leu))
ISCN -
DB-ID CHRND_000089
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) 1.0E-5 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2025-11-01 13:22:20 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CHRND NM_000751.2 ?/. - c.11C>T r.(?) p.(Pro4Leu)
PRSS56 NM_001195129.1 ?/. - c.*720C>T r.(=) p.(=)


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