Variant #0000553630 (NC_000015.9:g.23086385_23086390dup, NM_144599.4:c.42_47dup (NIPA1))

Chromosome 15
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.23086385_23086390dup
DNA change (hg38) g.22786678_22786683dup
Published as NIPA1(NM_001142275.1):c.-48+455_-48+456insGGCGGC (p.(=)), NIPA1(NM_144599.4):c.36_41dupGGCGGC (p.A15_A16dup), NIPA1(NM_144599.5):c.36_41dupGGCGGC ...
ISCN -
DB-ID NIPA1_000011 See all 5 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_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2019-07-18 18:22:55 +02:00 (CEST)
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.42_47dup r.(?) p.(Ala15_Ala16dup)


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