Variant #0000960060 (NC_000007.13:g.142458412C>T, NM_002769.4:c.47C>T (PRSS1))

Chromosome 7
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.142458412C>T
DNA change (hg38) -
Published as -
ISCN -
DB-ID PRSS1_000044 See all 4 reported entries
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs202003805
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner MobiDetails
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by MobiDetails
Date created 2024-02-13 10:59:01 +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     
PRSS1 NM_002769.4 +/. - c.47C>T r.(?) p.(Ala16Val)


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