Variant #0000855189 (NC_000017.10:g.8925724_8925732del, NM_004822.2:c.34_42del (NTN1))

Chromosome 17
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.8925724_8925732del
DNA change (hg38) -
Published as NTN1(NM_004822.3):c.34_42delCTGGCGGCG (p.L12_A14del)
ISCN -
DB-ID NTN1_000017
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_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2022-05-09 15:47:41 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
NTN1 NM_004822.2 ?/. - c.34_42del r.(?) p.(Leu12_Ala14del)


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