Variant #0001034380 (NC_000004.11:g.152097847G>A, NM_183375.2:c.-100478G>A (PRSS48))

Chromosome 4
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.152097847G>A
DNA change (hg38) -
Published as SH3D19(NM_001378122.1):c.376-8C>T
ISCN -
DB-ID PRSS48_000011
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) Retrieve
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2025-05-05 21:14:00 +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     
SH3D19 NM_001009555.3 -?/. - c.-486-8C>T r.(=) p.(=)
PRSS48 NM_183375.2 -?/. - c.-100478G>A r.(?) p.(=)


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