Variant #0000254327 (NC_000016.9:g.31092186A>T, NM_001039503.2:c.*2925T>A (PRSS53))

Chromosome 16
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.31092186A>T
DNA change (hg38) g.31080865A>T
Published as ZNF646(NM_014699.3):c.4541A>T (p.D1514V)
ISCN -
DB-ID ZNF646_000005
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) 0.00015 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PRSS53 NM_001039503.2 -?/. - c.*2925T>A r.(=) p.(=)
ZNF646 NM_014699.3 -?/. - c.4541A>T r.(?) p.(Asp1514Val)
ZNF668 NM_024706.4 -?/. - c.-7229T>A r.(?) p.(=)


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