Variant #0000891967 (NC_000015.9:g.23086388_23086390del, NM_144599.4:c.45_47del (NIPA1))

Chromosome 15
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.23086388_23086390del
DNA change (hg38) -
Published as NIPA1(NM_001142275.1):c.-48+453_-48+455del (p.(=)), NIPA1(NM_144599.5):c.45_47delGGC (p.A16del)
ISCN -
DB-ID NIPA1_000012 See all 3 reported entries
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_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 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
NIPA1 NM_144599.4 -/. - c.45_47del r.(?) p.(Ala16del)


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