Variant #0000895380 (NC_000020.10:g.57234706T>C, NM_024663.3:c.-33251T>C (NPEPL1))

Chromosome 20
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.57234706T>C
DNA change (hg38) -
Published as STX16(NM_001001433.2):c.144+16T>C
ISCN -
DB-ID NPEPL1_000006
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) 0.00103 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2022-11-01 13:41:49 +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     
STX16 NM_001001433.2 -?/. - c.144+16T>C r.(=) p.(=)
STX16 NM_003763.5 -?/. - c.81+7563T>C r.(=) p.(=)
NPEPL1 NM_024663.3 -?/. - c.-33251T>C r.(?) p.(=)
STX16-NPEPL1 NR_037945.1 -?/. - n.898+16T>C r.(?) -


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