Variant #0000975091 (NC_000002.11:g.233388535C>A, NM_000751.2:c.-2391C>A (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.233388535C>A
DNA change (hg38) -
Published as PRSS56(NM_001195129.1):c.1066C>A (p.Q356K), PRSS56(NM_001195129.2):c.1066C>A (p.(Gln356Lys))
ISCN -
DB-ID CHRND_000058 See all 2 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) 3.0E-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 2024-04-19 20:20:39 +02:00 (CEST)
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.-2391C>A r.(?) p.(=)
PRSS56 NM_001195129.1 ?/. - c.1066C>A r.(?) p.(Gln356Lys)


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