Variant #0000931188 (NC_000020.10:g.57227178C>G, NM_024663.3:c.-40779C>G (NPEPL1))

Chromosome 20
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.57227178C>G
DNA change (hg38) -
Published as STX16(NM_001001433.3):c.116C>G (p.S39*)
ISCN -
DB-ID NPEPL1_000009
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_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2023-07-07 10:10:56 +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     
STX16 NM_001001433.2 ?/. - c.116C>G r.(?) p.(Ser39*)
STX16 NM_003763.5 ?/. - c.81+35C>G r.(=) p.(=)
NPEPL1 NM_024663.3 ?/. - c.-40779C>G r.(?) p.(=)
STX16-NPEPL1 NR_037945.1 ?/. - n.870C>G r.(?) -


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